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Which methods support the evidence found for the SNV1063000? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1063000? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1063000, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1063000, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1063000? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1063000? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1063000? | The origin is germline. | <s>[INST] What is the origin for SNV1063000? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1063000? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1063000? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1063000? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1063000? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1063003? | 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/RsSNV1063003. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1063003. | <s>[INST] Which condition is asociated with SNV1063003? [/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/RsSNV1063003. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1063003. </s> |
In which chromosome is SNV1063003 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1063003 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1063003? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1063003? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1063003, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1063003, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1063003? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1063003? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1063003? | The origin is germline. | <s>[INST] What is the origin for SNV1063003? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1063003? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1063003? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1063003? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV1063003? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV1063010? | 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/RsSNV1063010. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1063010. | <s>[INST] Which condition is asociated with SNV1063010? [/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/RsSNV1063010. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1063010. </s> |
In which chromosome is SNV1063010 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1063010 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1063010? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1063010? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1063010, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1063010, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1063010? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1063010? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1063010? | The origin is germline. | <s>[INST] What is the origin for SNV1063010? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1063010? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1063010? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1063010? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1063010? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV983593? | 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/RsSNV983593. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983593. | <s>[INST] Which condition is asociated with SNV983593? [/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/RsSNV983593. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983593. </s> |
In which chromosome is SNV983593 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV983593 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV983593? | Associated methods are: research, clinical testing. | <s>[INST] Which methods support the evidence found for the SNV983593? [/INST] Associated methods are: research, clinical testing. </s> |
What is the clinical significance of SNV983593, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV983593, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV983593? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV983593? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV983593? | The origin is germline. | <s>[INST] What is the origin for SNV983593? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV983593? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV983593? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV983593? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for SNV983593? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV983600? | 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/RsSNV983600. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983600. | <s>[INST] Which condition is asociated with SNV983600? [/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/RsSNV983600. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983600. </s> |
In which chromosome is SNV983600 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV983600 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV983600? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the SNV983600? [/INST] Associated methods are: research. </s> |
What is the clinical significance of SNV983600, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV983600, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV983600? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV983600? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV983600? | The origin is germline. | <s>[INST] What is the origin for SNV983600? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV983600? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV983600? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV983600? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV983600? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV983591? | 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/RsSNV983591. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983591. | <s>[INST] Which condition is asociated with SNV983591? [/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/RsSNV983591. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983591. </s> |
In which chromosome is SNV983591 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV983591 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV983591? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the SNV983591? [/INST] Associated methods are: research. </s> |
What is the clinical significance of SNV983591, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV983591, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV983591? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV983591? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV983591? | The origin is germline. | <s>[INST] What is the origin for SNV983591? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV983591? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV983591? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV983591? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV983591? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1166992? | 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/RsSNV1166992. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1166992. | <s>[INST] Which condition is asociated with SNV1166992? [/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/RsSNV1166992. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1166992. </s> |
In which chromosome is SNV1166992 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1166992 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1166992? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1166992? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1166992, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1166992, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1166992? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1166992? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1166992? | The origin is germline. | <s>[INST] What is the origin for SNV1166992? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1166992? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1166992? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1166992? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1166992? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1166996? | 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/RsSNV1166996. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1166996. | <s>[INST] Which condition is asociated with SNV1166996? [/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/RsSNV1166996. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1166996. </s> |
In which chromosome is SNV1166996 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1166996 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1166996? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1166996? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1166996, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1166996, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1166996? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1166996? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1166996? | The origin is germline. | <s>[INST] What is the origin for SNV1166996? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1166996? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1166996? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1166996? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for SNV1166996? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS3020646 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/RsRS3020646 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS3020646 SNP. | <s>[INST] Which condition is asociated with RS3020646 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/RsRS3020646 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS3020646 SNP. </s> |
In which chromosome is RS3020646 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS3020646 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS3020646 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS3020646 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS3020646 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS3020646 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS3020646 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS3020646 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS3020646 SNP? | The origin is germline. | <s>[INST] What is the origin for RS3020646 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS3020646 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS3020646 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS3020646 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS3020646 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS198617 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/RsRS198617 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS198617 SNP. | <s>[INST] Which condition is asociated with RS198617 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/RsRS198617 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS198617 SNP. </s> |
In which chromosome is RS198617 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS198617 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS198617 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS198617 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS198617 SNP, is it benign or pathogenic? | It is Benign. | <s>[INST] What is the clinical significance of RS198617 SNP, is it benign or pathogenic? [/INST] It is Benign. </s> |
How long is the variation length for RS198617 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS198617 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS198617 SNP? | The origin is germline. | <s>[INST] What is the origin for RS198617 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS198617 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS198617 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS198617 SNP? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for RS198617 SNP? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with RS1131690882 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/RsRS1131690882 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690882 SNP. | <s>[INST] Which condition is asociated with RS1131690882 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/RsRS1131690882 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690882 SNP. </s> |
In which chromosome is RS1131690882 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1131690882 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1131690882 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1131690882 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1131690882 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1131690882 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1131690882 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1131690882 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1131690882 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1131690882 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1131690882 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1131690882 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1131690882 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1131690882 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with RS1131690907 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/RsRS1131690907 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690907 SNP. | <s>[INST] Which condition is asociated with RS1131690907 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/RsRS1131690907 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1131690907 SNP. </s> |
In which chromosome is RS1131690907 SNP located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is RS1131690907 SNP located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the RS1131690907 SNP? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the RS1131690907 SNP? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of RS1131690907 SNP, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of RS1131690907 SNP, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for RS1131690907 SNP? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for RS1131690907 SNP? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for RS1131690907 SNP? | The origin is germline. | <s>[INST] What is the origin for RS1131690907 SNP? [/INST] The origin is germline. </s> |
What is the type of genetic variation for RS1131690907 SNP? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for RS1131690907 SNP? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for RS1131690907 SNP? | The resulting gene consequence is a splice donor variant. | <s>[INST] What is the genetic molecular consequence for RS1131690907 SNP? [/INST] The resulting gene consequence is a splice donor variant. </s> |
Which condition is asociated with SNV1409060? | 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/RsSNV1409060. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1409060. | <s>[INST] Which condition is asociated with SNV1409060? [/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/RsSNV1409060. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1409060. </s> |
In which chromosome is SNV1409060 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1409060 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1409060? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1409060? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1409060, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1409060, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1409060? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1409060? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1409060? | The origin is germline. | <s>[INST] What is the origin for SNV1409060? [/INST] The origin is germline. </s> |