| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
C | 0.700 | CausalMutation | CLINVAR | Recurrent mutations of BRCA1 and BRCA2 in Poland: an update. | 24528374 | 2015 |
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|
C | 0.700 | CausalMutation | CLINVAR | Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence. | 23479189 | 2013 |
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|
C | 0.700 | CausalMutation | CLINVAR | BRCA1/BRCA2 gene mutations/SNPs and BRCA1 haplotypes in early-onset breast cancer patients of Indian ethnicity. | 22752604 | 2012 |
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|
C | 0.700 | CausalMutation | CLINVAR | BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. | 21952622 | 2011 |
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|
C | 0.700 | CausalMutation | CLINVAR | Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. | 21324516 | 2011 |
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|
C | 0.700 | CausalMutation | CLINVAR | Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. | 23199084 | 2010 |
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|
C | 0.700 | CausalMutation | CLINVAR | Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study. | 20104584 | 2010 |
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|
C | 0.700 | CausalMutation | CLINVAR | Cross-sectional analysis of germline BRCA1 and BRCA2 mutations in Japanese patients suspected to have hereditary breast/ovarian cancer. | 19016756 | 2008 |
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|
C | 0.700 | CausalMutation | CLINVAR | The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. | 8589730 | 1996 |