| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
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 | BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families. | 23767878 | 2013 |
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|
C | 0.700 | CausalMutation | CLINVAR | Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ. | 22009639 | 2012 |
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|
C | 0.700 | CausalMutation | CLINVAR | Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management. | 22535016 | 2012 |
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|
C | 0.700 | CausalMutation | CLINVAR | Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes. | 17513806 | 2007 |
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|
C | 0.700 | CausalMutation | CLINVAR | Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. | 16825431 | 2007 |
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|
C | 0.700 | CausalMutation | CLINVAR | Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years. | 16912212 | 2006 |
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|
C | 0.700 | CausalMutation | CLINVAR | A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer. | 14647210 | 2003 |
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|
C | 0.700 | CausalMutation | CLINVAR | Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. | 9667259 | 1998 |