Source: INFERRED ×
Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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|
G | 0.700 | CausalMutation | CLINVAR | Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes. | 24549055 | 2014 |
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|
G | 0.700 | CausalMutation | CLINVAR | Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer. | 23569316 | 2013 |
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|
G | 0.700 | CausalMutation | CLINVAR | BRCA1 and BRCA2 mutations among ovarian cancer patients from Colombia. | 22044689 | 2012 |
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|
G | 0.700 | CausalMutation | CLINVAR | BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma. | 17624602 | 2007 |
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|
G | 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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|
G | 0.700 | CausalMutation | CLINVAR | Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ. | 15728167 | 2005 |
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|
G | 0.700 | CausalMutation | CLINVAR | Cancer variation associated with the position of the mutation in the BRCA2 gene. | 15131399 | 2004 |
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|
G | 0.700 | CausalMutation | CLINVAR | Individual and family characteristics associated with protein truncating BRCA1 and BRCA2 mutations in an Ontario population based series from the Cooperative Family Registry for Breast Cancer Studies. | 12920083 | 2003 |
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|
G | 0.700 | CausalMutation | CLINVAR | BRCA1 and BRCA2 mutations in central and southern Italian patients. | 11056688 | 2000 |
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|
A | 0.700 | CausalMutation | CLINVAR |