Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
A | 0.700 | CausalMutation | CLINVAR | Fanconi anemia: at the crossroads of DNA repair. | 21568838 | 2011 |
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|
A | 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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|
A | 0.700 | CausalMutation | CLINVAR | Breast cancer risk among male BRCA1 and BRCA2 mutation carriers. | 18042939 | 2007 |
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|
A | 0.700 | CausalMutation | CLINVAR | Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. | 16825431 | 2007 |
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|
A | 0.700 | CausalMutation | CLINVAR | Meta-analysis of BRCA1 and BRCA2 penetrance. | 17416853 | 2007 |
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|
A | 0.700 | CausalMutation | CLINVAR | BRCA1 and pancreatic cancer: pedigree findings and their causal relationships. | 15796958 | 2005 |
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|
A | 0.700 | CausalMutation | CLINVAR | Cancer risks in BRCA2 families: estimates for sites other than breast and ovary. | 16141007 | 2005 |
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|
A | 0.700 | CausalMutation | CLINVAR | Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers. | 15197194 | 2004 |
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|
A | 0.700 | CausalMutation | CLINVAR | Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. | 12677558 | 2003 |
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|
A | 0.700 | CausalMutation | CLINVAR | Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. | 9497246 | 1998 |