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What is the genetic molecular consequence for RS137853295 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS137853295 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS587776790 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587776790 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776790 SNP. | <s>[INST] Which condition is asociated with RS587776790 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587776790 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776790 SNP. </s> |
In which chromosome is RS587776790 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587776790 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587776790 SNP? | Associated methods are: literature only. | <s>[INST] Which methods support the evidence found for the RS587776790 SNP? [/INST] Associated methods are: literature only. </s> |
What is the clinical significance of RS587776790 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587776790 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587776790 SNP? | The variation length is 23 base pairs. | <s>[INST] How long is the variation length for RS587776790 SNP? [/INST] The variation length is 23 base pairs. </s> |
What is the origin for RS587776790 SNP? | The origin is germline. | <s>[INST] What is the origin for RS587776790 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS587776790 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS587776790 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS587776790 SNP? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for RS587776790 SNP? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with RS587776791 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587776791 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776791 SNP. | <s>[INST] Which condition is asociated with RS587776791 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587776791 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587776791 SNP. </s> |
In which chromosome is RS587776791 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587776791 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587776791 SNP? | Associated methods are: literature only. | <s>[INST] Which methods support the evidence found for the RS587776791 SNP? [/INST] Associated methods are: literature only. </s> |
What is the clinical significance of RS587776791 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587776791 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587776791 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587776791 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587776791 SNP? | The origin is germline. | <s>[INST] What is the origin for RS587776791 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS587776791 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587776791 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587776791 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS587776791 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS587778858 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778858 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778858 SNP. | <s>[INST] Which condition is asociated with RS587778858 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778858 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778858 SNP. </s> |
In which chromosome is RS587778858 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778858 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778858 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778858 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778858 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778858 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778858 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778858 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778858 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778858 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778858 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778858 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778858 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS587778858 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS1566233014 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1566233014 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566233014 SNP. | <s>[INST] Which condition is asociated with RS1566233014 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1566233014 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566233014 SNP. </s> |
In which chromosome is RS1566233014 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1566233014 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1566233014 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS1566233014 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS1566233014 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1566233014 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1566233014 SNP? | The variation length is None base pairs. | <s>[INST] How long is the variation length for RS1566233014 SNP? [/INST] The variation length is None base pairs. </s> |
What is the origin for RS1566233014 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS1566233014 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS1566233014 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS1566233014 SNP? [/INST] The variation is a Duplication. </s> |
Which condition is asociated with RS587778833 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778833 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778833 SNP. | <s>[INST] Which condition is asociated with RS587778833 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778833 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778833 SNP. </s> |
In which chromosome is RS587778833 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778833 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778833 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS587778833 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS587778833 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778833 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778833 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778833 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778833 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778833 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778833 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778833 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778833 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS587778833 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS587778865 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778865 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778865 SNP. | <s>[INST] Which condition is asociated with RS587778865 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778865 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778865 SNP. </s> |
In which chromosome is RS587778865 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778865 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778865 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS587778865 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS587778865 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778865 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778865 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778865 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778865 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778865 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778865 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778865 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778865 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS587778865 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS587778866 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778866 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778866 SNP. | <s>[INST] Which condition is asociated with RS587778866 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778866 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778866 SNP. </s> |
In which chromosome is RS587778866 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778866 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778866 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS587778866 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS587778866 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778866 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778866 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778866 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778866 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778866 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778866 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778866 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778866 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS587778866 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS587778834 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778834 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778834 SNP. | <s>[INST] Which condition is asociated with RS587778834 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778834 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778834 SNP. </s> |
In which chromosome is RS587778834 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778834 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778834 SNP? | Associated methods are: research, clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778834 SNP? [/INST] Associated methods are: research, clinical testing. </s> |
What is the clinical significance of RS587778834 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS587778834 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS587778834 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778834 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778834 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778834 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778834 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778834 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778834 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS587778834 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS587778859 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778859 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778859 SNP. | <s>[INST] Which condition is asociated with RS587778859 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778859 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778859 SNP. </s> |
In which chromosome is RS587778859 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778859 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778859 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778859 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778859 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778859 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778859 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778859 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778859 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778859 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778859 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778859 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778859 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS587778859 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS587778835 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778835 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778835 SNP. | <s>[INST] Which condition is asociated with RS587778835 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778835 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778835 SNP. </s> |
In which chromosome is RS587778835 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778835 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778835 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778835 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778835 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778835 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778835 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778835 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778835 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778835 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778835 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778835 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778835 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS587778835 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS587778868 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778868 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778868 SNP. | <s>[INST] Which condition is asociated with RS587778868 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778868 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778868 SNP. </s> |
In which chromosome is RS587778868 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778868 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778868 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778868 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778868 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778868 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778868 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778868 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778868 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778868 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778868 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778868 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778868 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS587778868 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS587778861 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778861 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778861 SNP. | <s>[INST] Which condition is asociated with RS587778861 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778861 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778861 SNP. </s> |
In which chromosome is RS587778861 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778861 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778861 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778861 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778861 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778861 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS587778861 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS587778861 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS587778861 SNP? | The origin is somatic. | <s>[INST] What is the origin for RS587778861 SNP? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for RS587778861 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS587778861 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS587778861 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS587778861 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS587778826 SNP? | Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778826 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778826 SNP. | <s>[INST] Which condition is asociated with RS587778826 SNP? [/INST] Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS587778826 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778826 SNP. </s> |
In which chromosome is RS587778826 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS587778826 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS587778826 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS587778826 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS587778826 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS587778826 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |