Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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|
A | 0.700 | GeneticVariation | CLINVAR | Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. | 29394989 | 2018 |
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|
T | 0.700 | GeneticVariation | CLINVAR | Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational Approaches. | 29394989 | 2018 |
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|
T | 0.700 | GeneticVariation | CLINVAR | BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population? | 29161300 | 2017 |
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|
T | 0.700 | GeneticVariation | CLINVAR | Functional assays for analysis of variants of uncertain significance in BRCA2. | 24323938 | 2014 |
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|
A | 0.700 | GeneticVariation | CLINVAR | A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity. | 23108138 | 2013 |
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|
A | 0.700 | GeneticVariation | CLINVAR | BRCA germline mutations in Jewish patients with pancreatic adenocarcinoma. | 19064968 | 2009 |
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|
T | 0.700 | GeneticVariation | CLINVAR | Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios. | 19043619 | 2008 |
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|
A | 0.700 | GeneticVariation | CLINVAR | Classifying Variants of Undetermined Significance in BRCA2 with protein likelihood ratios. | 19043619 | 2008 |
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|
A | 0.700 | GeneticVariation | CLINVAR | BRCA2 germline mutations in familial pancreatic carcinoma. | 12569143 | 2003 |
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|
T | 0.700 | GeneticVariation | CLINVAR | BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure. | 12228710 | 2002 |
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|
A | 0.700 | GeneticVariation | CLINVAR | BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure. | 12228710 | 2002 |
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|
A | 0.700 | GeneticVariation | CLINVAR | Frequency of BRCA1 and BRCA2 germline mutations in Japanese breast cancer families. | 11149425 | 2001 |