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What is the genetic molecular consequence for RS1131690891 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1131690891 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS1952715820 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/RsRS1952715820 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952715820 SNP. | <s>[INST] Which condition is asociated with RS1952715820 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/RsRS1952715820 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1952715820 SNP. </s> |
In which chromosome is RS1952715820 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1952715820 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1952715820 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1952715820 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1952715820 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1952715820 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1952715820 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1952715820 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1952715820 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1952715820 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1952715820 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1952715820 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1952715820 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS1952715820 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS1593539386 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/RsRS1593539386 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539386 SNP. | <s>[INST] Which condition is asociated with RS1593539386 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/RsRS1593539386 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593539386 SNP. </s> |
In which chromosome is RS1593539386 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1593539386 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1593539386 SNP? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the RS1593539386 SNP? [/INST] Associated methods are: research. </s> |
What is the clinical significance of RS1593539386 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1593539386 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1593539386 SNP? | The variation length is 22 base pairs. | <s>[INST] How long is the variation length for RS1593539386 SNP? [/INST] The variation length is 22 base pairs. </s> |
What is the origin for RS1593539386 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1593539386 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1593539386 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS1593539386 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS1593539386 SNP? | The resulting gene consequence is a inframe_insertion. | <s>[INST] What is the genetic molecular consequence for RS1593539386 SNP? [/INST] The resulting gene consequence is a inframe_insertion. </s> |
Which condition is asociated with SNV1324868? | 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/RsSNV1324868. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1324868. | <s>[INST] Which condition is asociated with SNV1324868? [/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/RsSNV1324868. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1324868. </s> |
In which chromosome is SNV1324868 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1324868 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1324868? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1324868? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1324868, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of SNV1324868, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for SNV1324868? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1324868? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1324868? | The origin is somatic. | <s>[INST] What is the origin for SNV1324868? [/INST] The origin is somatic. </s> |
What is the type of genetic variation for SNV1324868? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1324868? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1324868? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for SNV1324868? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS1012377281 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/RsRS1012377281 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1012377281 SNP. | <s>[INST] Which condition is asociated with RS1012377281 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/RsRS1012377281 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1012377281 SNP. </s> |
In which chromosome is RS1012377281 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1012377281 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1012377281 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1012377281 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1012377281 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1012377281 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1012377281 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1012377281 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1012377281 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1012377281 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1012377281 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1012377281 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1012377281 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1012377281 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS1566194400 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/RsRS1566194400 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566194400 SNP. | <s>[INST] Which condition is asociated with RS1566194400 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/RsRS1566194400 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1566194400 SNP. </s> |
In which chromosome is RS1566194400 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1566194400 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1566194400 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1566194400 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1566194400 SNP, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of RS1566194400 SNP, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for RS1566194400 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1566194400 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1566194400 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1566194400 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1566194400 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1566194400 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1566194400 SNP? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for RS1566194400 SNP? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with RS1555283670 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/RsRS1555283670 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1555283670 SNP. | <s>[INST] Which condition is asociated with RS1555283670 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/RsRS1555283670 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1555283670 SNP. </s> |
In which chromosome is RS1555283670 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1555283670 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1555283670 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1555283670 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1555283670 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1555283670 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1555283670 SNP? | The variation length is 5 base pairs. | <s>[INST] How long is the variation length for RS1555283670 SNP? [/INST] The variation length is 5 base pairs. </s> |
What is the origin for RS1555283670 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1555283670 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1555283670 SNP? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for RS1555283670 SNP? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for RS1555283670 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS1555283670 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS1949430616 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/RsRS1949430616 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949430616 SNP. | <s>[INST] Which condition is asociated with RS1949430616 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/RsRS1949430616 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1949430616 SNP. </s> |
In which chromosome is RS1949430616 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1949430616 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1949430616 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1949430616 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1949430616 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1949430616 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1949430616 SNP? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for RS1949430616 SNP? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for RS1949430616 SNP? | The origin is unknown. | <s>[INST] What is the origin for RS1949430616 SNP? [/INST] The origin is unknown. </s> |
What is the type of genetic variation for RS1949430616 SNP? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for RS1949430616 SNP? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for RS1949430616 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS1949430616 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS121913297 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/RsRS121913297 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS121913297 SNP. | <s>[INST] Which condition is asociated with RS121913297 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/RsRS121913297 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS121913297 SNP. </s> |
In which chromosome is RS121913297 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS121913297 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS121913297 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS121913297 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS121913297 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS121913297 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS121913297 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS121913297 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS121913297 SNP? | The origin is germline. | <s>[INST] What is the origin for RS121913297 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS121913297 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS121913297 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS121913297 SNP? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for RS121913297 SNP? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with SNV1691098? | 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/RsSNV1691098. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691098. | <s>[INST] Which condition is asociated with SNV1691098? [/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/RsSNV1691098. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691098. </s> |
In which chromosome is SNV1691098 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1691098 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1691098? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1691098? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1691098, is it benign or pathogenic? | It is Uncertain significance. | <s>[INST] What is the clinical significance of SNV1691098, is it benign or pathogenic? [/INST] It is Uncertain significance. </s> |
How long is the variation length for SNV1691098? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1691098? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1691098? | The origin is germline. | <s>[INST] What is the origin for SNV1691098? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1691098? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1691098? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1691098? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for SNV1691098? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with SNV1691139? | 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/RsSNV1691139. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691139. | <s>[INST] Which condition is asociated with SNV1691139? [/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/RsSNV1691139. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691139. </s> |
In which chromosome is SNV1691139 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1691139 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1691139? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1691139? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1691139, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of SNV1691139, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for SNV1691139? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1691139? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1691139? | The origin is germline. | <s>[INST] What is the origin for SNV1691139? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1691139? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1691139? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1691139? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for SNV1691139? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with SNV1691303? | 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/RsSNV1691303. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691303. | <s>[INST] Which condition is asociated with SNV1691303? [/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/RsSNV1691303. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1691303. </s> |
In which chromosome is SNV1691303 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1691303 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1691303? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1691303? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1691303, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1691303, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1691303? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1691303? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1691303? | The origin is germline. | <s>[INST] What is the origin for SNV1691303? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1691303? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1691303? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1691303? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for SNV1691303? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with RS1131690859 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/RsRS1131690859 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690859 SNP. | <s>[INST] Which condition is asociated with RS1131690859 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/RsRS1131690859 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690859 SNP. </s> |
In which chromosome is RS1131690859 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1131690859 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1131690859 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1131690859 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1131690859 SNP, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of RS1131690859 SNP, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for RS1131690859 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1131690859 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1131690859 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1131690859 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1131690859 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1131690859 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1131690859 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS1131690859 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with SNV1860317? | 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/RsSNV1860317. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1860317. | <s>[INST] Which condition is asociated with SNV1860317? [/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/RsSNV1860317. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1860317. </s> |
In which chromosome is SNV1860317 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1860317 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1860317? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1860317? [/INST] Associated methods are: clinical testing. </s> |