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What is the type of genetic variation for SNV1052627? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1052627? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1052627? | The resulting gene consequence is a missense variant. | <s>[INST] What is the genetic molecular consequence for SNV1052627? [/INST] The resulting gene consequence is a missense variant. </s> |
Which condition is asociated with DEL1056155? | 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/RsDEL1056155. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1056155. | <s>[INST] Which condition is asociated with DEL1056155? [/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/RsDEL1056155. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1056155. </s> |
In which chromosome is DEL1056155 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1056155 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1056155? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1056155? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1056155, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of DEL1056155, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for DEL1056155? | The variation length is 8 base pairs. | <s>[INST] How long is the variation length for DEL1056155? [/INST] The variation length is 8 base pairs. </s> |
What is the origin for DEL1056155? | The origin is germline. | <s>[INST] What is the origin for DEL1056155? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1056155? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1056155? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with SNV1062988? | 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/RsSNV1062988. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062988. | <s>[INST] Which condition is asociated with SNV1062988? [/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/RsSNV1062988. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV1062988. </s> |
In which chromosome is SNV1062988 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV1062988 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV1062988? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the SNV1062988? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of SNV1062988, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of SNV1062988, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for SNV1062988? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV1062988? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV1062988? | The origin is germline. | <s>[INST] What is the origin for SNV1062988? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV1062988? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV1062988? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV1062988? | The resulting gene consequence is a nonsense. | <s>[INST] What is the genetic molecular consequence for SNV1062988? [/INST] The resulting gene consequence is a nonsense. </s> |
Which condition is asociated with DEL1057629? | 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/RsDEL1057629. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1057629. | <s>[INST] Which condition is asociated with DEL1057629? [/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/RsDEL1057629. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1057629. </s> |
In which chromosome is DEL1057629 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1057629 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1057629? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1057629? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1057629, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL1057629, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL1057629? | The variation length is 176357 base pairs. | <s>[INST] How long is the variation length for DEL1057629? [/INST] The variation length is 176357 base pairs. </s> |
What is the origin for DEL1057629? | The origin is germline. | <s>[INST] What is the origin for DEL1057629? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1057629? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1057629? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DEL1062987? | 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/RsDEL1062987. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1062987. | <s>[INST] Which condition is asociated with DEL1062987? [/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/RsDEL1062987. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1062987. </s> |
In which chromosome is DEL1062987 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1062987 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1062987? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1062987? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1062987, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL1062987, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL1062987? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DEL1062987? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DEL1062987? | The origin is germline. | <s>[INST] What is the origin for DEL1062987? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1062987? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1062987? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for DEL1062987? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DEL1062987? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL1062993? | 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/RsDEL1062993. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1062993. | <s>[INST] Which condition is asociated with DEL1062993? [/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/RsDEL1062993. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1062993. </s> |
In which chromosome is DEL1062993 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1062993 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1062993? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1062993? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1062993, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL1062993, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL1062993? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DEL1062993? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DEL1062993? | The origin is germline. | <s>[INST] What is the origin for DEL1062993? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1062993? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1062993? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for DEL1062993? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DEL1062993? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL1057630? | 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/RsDEL1057630. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1057630. | <s>[INST] Which condition is asociated with DEL1057630? [/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/RsDEL1057630. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL1057630. </s> |
In which chromosome is DEL1057630 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL1057630 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL1057630? | Associated methods are: clinical testing. | <s>[INST] Which methods support the evidence found for the DEL1057630? [/INST] Associated methods are: clinical testing. </s> |
What is the clinical significance of DEL1057630, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL1057630, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL1057630? | The variation length is 41307 base pairs. | <s>[INST] How long is the variation length for DEL1057630? [/INST] The variation length is 41307 base pairs. </s> |
What is the origin for DEL1057630? | The origin is germline. | <s>[INST] What is the origin for DEL1057630? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL1057630? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL1057630? [/INST] The variation is a Deletion. </s> |
Which condition is asociated with DUP983595? | 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/RsDUP983595. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP983595. | <s>[INST] Which condition is asociated with DUP983595? [/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/RsDUP983595. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP983595. </s> |
In which chromosome is DUP983595 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP983595 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP983595? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the DUP983595? [/INST] Associated methods are: research. </s> |
What is the clinical significance of DUP983595, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DUP983595, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DUP983595? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for DUP983595? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for DUP983595? | The origin is germline. | <s>[INST] What is the origin for DUP983595? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP983595? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP983595? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for DUP983595? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DUP983595? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DUP983596? | 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/RsDUP983596. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP983596. | <s>[INST] Which condition is asociated with DUP983596? [/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/RsDUP983596. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DUP983596. </s> |
In which chromosome is DUP983596 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DUP983596 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DUP983596? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the DUP983596? [/INST] Associated methods are: research. </s> |
What is the clinical significance of DUP983596, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DUP983596, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DUP983596? | The variation length is 11 base pairs. | <s>[INST] How long is the variation length for DUP983596? [/INST] The variation length is 11 base pairs. </s> |
What is the origin for DUP983596? | The origin is germline. | <s>[INST] What is the origin for DUP983596? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DUP983596? | The variation is a Duplication. | <s>[INST] What is the type of genetic variation for DUP983596? [/INST] The variation is a Duplication. </s> |
What is the genetic molecular consequence for DUP983596? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DUP983596? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with DEL983588? | 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/RsDEL983588. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL983588. | <s>[INST] Which condition is asociated with DEL983588? [/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/RsDEL983588. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/DEL983588. </s> |
In which chromosome is DEL983588 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is DEL983588 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the DEL983588? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the DEL983588? [/INST] Associated methods are: research. </s> |
What is the clinical significance of DEL983588, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of DEL983588, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for DEL983588? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for DEL983588? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for DEL983588? | The origin is germline. | <s>[INST] What is the origin for DEL983588? [/INST] The origin is germline. </s> |
What is the type of genetic variation for DEL983588? | The variation is a Deletion. | <s>[INST] What is the type of genetic variation for DEL983588? [/INST] The variation is a Deletion. </s> |
What is the genetic molecular consequence for DEL983588? | The resulting gene consequence is a frameshift variant. | <s>[INST] What is the genetic molecular consequence for DEL983588? [/INST] The resulting gene consequence is a frameshift variant. </s> |
Which condition is asociated with IND983589? | 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/RsIND983589. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/IND983589. | <s>[INST] Which condition is asociated with IND983589? [/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/RsIND983589. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/IND983589. </s> |
In which chromosome is IND983589 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is IND983589 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the IND983589? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the IND983589? [/INST] Associated methods are: research. </s> |
What is the clinical significance of IND983589, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of IND983589, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for IND983589? | The variation length is 2 base pairs. | <s>[INST] How long is the variation length for IND983589? [/INST] The variation length is 2 base pairs. </s> |
What is the origin for IND983589? | The origin is germline. | <s>[INST] What is the origin for IND983589? [/INST] The origin is germline. </s> |
What is the type of genetic variation for IND983589? | The variation is a Indel. | <s>[INST] What is the type of genetic variation for IND983589? [/INST] The variation is a Indel. </s> |
What is the genetic molecular consequence for IND983589? | The resulting gene consequence is a splice acceptor variant. | <s>[INST] What is the genetic molecular consequence for IND983589? [/INST] The resulting gene consequence is a splice acceptor variant. </s> |
Which condition is asociated with SNV983602? | 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/RsSNV983602. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983602. | <s>[INST] Which condition is asociated with SNV983602? [/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/RsSNV983602. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/SNV983602. </s> |
In which chromosome is SNV983602 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is SNV983602 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the SNV983602? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the SNV983602? [/INST] Associated methods are: research. </s> |
What is the clinical significance of SNV983602, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of SNV983602, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for SNV983602? | The variation length is 1 base pairs. | <s>[INST] How long is the variation length for SNV983602? [/INST] The variation length is 1 base pairs. </s> |
What is the origin for SNV983602? | The origin is germline. | <s>[INST] What is the origin for SNV983602? [/INST] The origin is germline. </s> |
What is the type of genetic variation for SNV983602? | The variation is a single nucleotide variant. | <s>[INST] What is the type of genetic variation for SNV983602? [/INST] The variation is a single nucleotide variant. </s> |
What is the genetic molecular consequence for SNV983602? | The resulting gene consequence is a intron variant. | <s>[INST] What is the genetic molecular consequence for SNV983602? [/INST] The resulting gene consequence is a intron variant. </s> |
Which condition is asociated with IND983582? | 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/RsIND983582. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/IND983582. | <s>[INST] Which condition is asociated with IND983582? [/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/RsIND983582. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/IND983582. </s> |
In which chromosome is IND983582 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is IND983582 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the IND983582? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the IND983582? [/INST] Associated methods are: research. </s> |
What is the clinical significance of IND983582, is it benign or pathogenic? | It is Likely pathogenic. | <s>[INST] What is the clinical significance of IND983582, is it benign or pathogenic? [/INST] It is Likely pathogenic. </s> |
How long is the variation length for IND983582? | The variation length is None base pairs. | <s>[INST] How long is the variation length for IND983582? [/INST] The variation length is None base pairs. </s> |
What is the origin for IND983582? | The origin is germline. | <s>[INST] What is the origin for IND983582? [/INST] The origin is germline. </s> |
What is the type of genetic variation for IND983582? | The variation is a Indel. | <s>[INST] What is the type of genetic variation for IND983582? [/INST] The variation is a Indel. </s> |
Which condition is asociated with 983601? | 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/Rs983601. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/983601. | <s>[INST] Which condition is asociated with 983601? [/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/Rs983601. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/983601. </s> |
In which chromosome is 983601 located? | It is located in the chromosome 13. | <s>[INST] In which chromosome is 983601 located? [/INST] It is located in the chromosome 13. </s> |
Which methods support the evidence found for the 983601? | Associated methods are: research. | <s>[INST] Which methods support the evidence found for the 983601? [/INST] Associated methods are: research. </s> |
What is the clinical significance of 983601, is it benign or pathogenic? | It is Pathogenic. | <s>[INST] What is the clinical significance of 983601, is it benign or pathogenic? [/INST] It is Pathogenic. </s> |
How long is the variation length for 983601? | The variation length is 4 base pairs. | <s>[INST] How long is the variation length for 983601? [/INST] The variation length is 4 base pairs. </s> |
What is the origin for 983601? | The origin is germline. | <s>[INST] What is the origin for 983601? [/INST] The origin is germline. </s> |