Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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|
C | 0.700 | GeneticVariation | CLINVAR | Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer. | 22798144 | 2012 |
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C | 0.700 | GeneticVariation | CLINVAR | BRCA1/BRCA2 mutation status and clinical-pathologic features of 108 male breast cancer cases from Tuscany: a population-based study in central Italy. | 18819001 | 2009 |
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C | 0.700 | GeneticVariation | CLINVAR | Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy. | 18821011 | 2009 |
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|
C | 0.700 | GeneticVariation | CLINVAR | Genetic epidemiology of BRCA mutations--family history detects less than 50% of the mutation carriers. | 17574839 | 2007 |
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C | 0.700 | GeneticVariation | CLINVAR | Founder mutations in BRCA1 and BRCA2 genes. | 17591843 | 2007 |
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|
C | 0.700 | GeneticVariation | CLINVAR | BRCA1 mutations in ovarian cancer and borderline tumours in Norway: a nested case-control study. | 15477862 | 2004 |
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|
C | 0.700 | GeneticVariation | CLINVAR | The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer. | 14522380 | 2003 |
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|
C | 0.700 | GeneticVariation | CLINVAR | Characterization of ten novel and 13 recurring BRCA1 and BRCA2 germline mutations in Italian breast and/or ovarian carcinoma patients. Mutations in brief no. 178. Online. | 10660329 | 1998 |
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|
C | 0.700 | CausalMutation | CLINVAR |