| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
C | 0.700 | CausalMutation | CLINVAR | Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. | 28724667 | 2017 |
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|
C | 0.700 | CausalMutation | CLINVAR | BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers. | 28831036 | 2017 |
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|
C | 0.700 | CausalMutation | CLINVAR | High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients. | 27553291 | 2016 |
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|
C | 0.700 | CausalMutation | CLINVAR | Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. | 24504028 | 2014 |
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|
C | 0.700 | CausalMutation | CLINVAR | Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease. | 24556621 | 2014 |
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|
C | 0.700 | CausalMutation | CLINVAR | BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations. | 16455195 | 2007 |
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|
C | 0.700 | CausalMutation | CLINVAR | Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer. | 17100994 | 2006 |
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|
C | 0.700 | CausalMutation | CLINVAR | Detection of BRCA1 and BRCA2 mutations in breast cancer families by a comprehensive two-stage screening procedure. | 10699917 | 2000 |
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|
C | 0.700 | CausalMutation | CLINVAR | BRCA1 mutations in a population-based sample of young women with breast cancer. | 8531967 | 1996 |
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|
C | 0.700 | CausalMutation | CLINVAR | A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening. | 7837387 | 1995 |