Source: CLINVAR ×
Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
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|
T | 0.700 | CausalMutation | CLINVAR | Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. | 25186627 | 2015 |
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|
T | 0.700 | CausalMutation | CLINVAR | Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ. | 22009639 | 2012 |
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|
T | 0.700 | CausalMutation | CLINVAR | Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2 deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age. | 20807450 | 2010 |
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|
T | 0.700 | CausalMutation | CLINVAR | Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer. | 18627636 | 2008 |