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What is the type of genetic variation for 983601? | The variation is a Microsatellite. | <s>[INST] What is the type of genetic variation for 983601? [/INST] The variation is a Microsatellite. </s> |
What is the genetic molecular consequence for 983601? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for 983601? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with SNV983594? | 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/RsSNV983594. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983594. | <s>[INST] Which condition is asociated with SNV983594? [/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/RsSNV983594. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983594. </s> |
In which chromosome is SNV983594 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV983594 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV983594? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the SNV983594? [/INST] Associated methods are: research. </s> |
What is the clinical significance of SNV983594, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV983594, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV983594? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV983594? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV983594? | The origin is germline. | <s>[INST] What is the origin for SNV983594? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV983594? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV983594? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV983594? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for SNV983594? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with DUP983590? | 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/RsDUP983590. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP983590. | <s>[INST] Which condition is asociated with DUP983590? [/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/RsDUP983590. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP983590. </s> |
In which chromosome is DUP983590 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP983590 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP983590? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the DUP983590? [/INST] Associated methods are: research. </s> |
What is the clinical significance of DUP983590, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DUP983590, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DUP983590? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DUP983590? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DUP983590? | The origin is germline. | <s>[INST] What is the origin for DUP983590? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP983590? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP983590? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for DUP983590? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DUP983590? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL983587? | 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/RsDEL983587. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL983587. | <s>[INST] Which condition is asociated with DEL983587? [/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/RsDEL983587. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL983587. </s> |
In which chromosome is DEL983587 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL983587 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL983587? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the DEL983587? [/INST] Associated methods are: research. </s> |
What is the clinical significance of DEL983587, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of DEL983587, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for DEL983587? | The variation length is 18 base pairs. | <s>[INST] How long is the variation length for DEL983587? [/INST] The variation length is 18 base pairs. </s> |
What is the origin for DEL983587? | The origin is germline. | <s>[INST] What is the origin for DEL983587? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL983587? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL983587? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL983597? | 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/RsDEL983597. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL983597. | <s>[INST] Which condition is asociated with DEL983597? [/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/RsDEL983597. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL983597. </s> |
In which chromosome is DEL983597 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL983597 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL983597? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the DEL983597? [/INST] Associated methods are: research. </s> |
What is the clinical significance of DEL983597, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL983597, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL983597? | The variation length is 5 base pairs. | <s>[INST] How long is the variation length for DEL983597? [/INST] The variation length is 5 base pairs. </s> |
What is the origin for DEL983597? | The origin is germline. | <s>[INST] What is the origin for DEL983597? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL983597? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL983597? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for DEL983597? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DEL983597? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with SNV983598? | 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/RsSNV983598. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983598. | <s>[INST] Which condition is asociated with SNV983598? [/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/RsSNV983598. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983598. </s> |
In which chromosome is SNV983598 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV983598 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV983598? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the SNV983598? [/INST] Associated methods are: research. </s> |
What is the clinical significance of SNV983598, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV983598, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV983598? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV983598? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV983598? | The origin is germline. | <s>[INST] What is the origin for SNV983598? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV983598? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV983598? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV983598? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for SNV983598? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with INS1166991? | 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/RsINS1166991. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/INS1166991. | <s>[INST] Which condition is asociated with INS1166991? [/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/RsINS1166991. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/INS1166991. </s> |
In which chromosome is INS1166991 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is INS1166991 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the INS1166991? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the INS1166991? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of INS1166991, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of INS1166991, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for INS1166991? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for INS1166991? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for INS1166991? | The origin is germline. | <s>[INST] What is the origin for INS1166991? [/INST] The origin is germline. </s> |
What is the type of genetic variation for INS1166991? | The variation is a Insertion. | <s>[INST] What is the type of genetic variation for INS1166991? [/INST] The variation is a Insertion. </s> |
What is the genetic molecular consequence for INS1166991? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for INS1166991? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL1166993? | 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/RsDEL1166993. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1166993. | <s>[INST] Which condition is asociated with DEL1166993? [/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/RsDEL1166993. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1166993. </s> |
In which chromosome is DEL1166993 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1166993 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1166993? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1166993? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1166993, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL1166993, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL1166993? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DEL1166993? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DEL1166993? | The origin is germline. | <s>[INST] What is the origin for DEL1166993? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1166993? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1166993? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for DEL1166993? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DEL1166993? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DUP1166994? | 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/RsDUP1166994. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP1166994. | <s>[INST] Which condition is asociated with DUP1166994? [/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/RsDUP1166994. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP1166994. </s> |
In which chromosome is DUP1166994 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP1166994 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP1166994? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DUP1166994? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DUP1166994, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DUP1166994, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DUP1166994? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DUP1166994? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DUP1166994? | The origin is germline. | <s>[INST] What is the origin for DUP1166994? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP1166994? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP1166994? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for DUP1166994? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DUP1166994? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DUP1166995? | 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/RsDUP1166995. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP1166995. | <s>[INST] Which condition is asociated with DUP1166995? [/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/RsDUP1166995. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP1166995. </s> |
In which chromosome is DUP1166995 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP1166995 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP1166995? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DUP1166995? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DUP1166995, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DUP1166995, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DUP1166995? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DUP1166995? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DUP1166995? | The origin is germline. | <s>[INST] What is the origin for DUP1166995? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP1166995? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP1166995? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for DUP1166995? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DUP1166995? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL1166997? | 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/RsDEL1166997. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1166997. | <s>[INST] Which condition is asociated with DEL1166997? [/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/RsDEL1166997. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1166997. </s> |
In which chromosome is DEL1166997 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1166997 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1166997? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1166997? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1166997, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL1166997, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL1166997? | The variation length is 4 base pairs. | <s>[INST] How long is the variation length for DEL1166997? [/INST] The variation length is 4 base pairs. </s> |
What is the origin for DEL1166997? | The origin is germline. | <s>[INST] What is the origin for DEL1166997? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1166997? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1166997? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for DEL1166997? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DEL1166997? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DUP1166998? | 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/RsDUP1166998. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP1166998. | <s>[INST] Which condition is asociated with DUP1166998? [/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/RsDUP1166998. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP1166998. </s> |
In which chromosome is DUP1166998 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP1166998 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP1166998? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DUP1166998? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DUP1166998, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DUP1166998, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DUP1166998? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DUP1166998? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DUP1166998? | The origin is germline. | <s>[INST] What is the origin for DUP1166998? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP1166998? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP1166998? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for DUP1166998? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DUP1166998? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with INS1166999? | 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/RsINS1166999. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/INS1166999. | <s>[INST] Which condition is asociated with INS1166999? [/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/RsINS1166999. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/INS1166999. </s> |
In which chromosome is INS1166999 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is INS1166999 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the INS1166999? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the INS1166999? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of INS1166999, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of INS1166999, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for INS1166999? | The variation length is 4 base pairs. | <s>[INST] How long is the variation length for INS1166999? [/INST] The variation length is 4 base pairs. </s> |
What is the origin for INS1166999? | The origin is germline. | <s>[INST] What is the origin for INS1166999? [/INST] The origin is germline. </s> |
What is the type of genetic variation for INS1166999? | The variation is a Insertion. | <s>[INST] What is the type of genetic variation for INS1166999? [/INST] The variation is a Insertion. </s> |
What is the genetic molecular consequence for INS1166999? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for INS1166999? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL1167000? | 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/RsDEL1167000. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1167000. | <s>[INST] Which condition is asociated with DEL1167000? [/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/RsDEL1167000. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1167000. </s> |
In which chromosome is DEL1167000 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1167000 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1167000? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1167000? [/INST] Associated methods are: clinical testing. </s> |