| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
A | 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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|
A | 0.700 | CausalMutation | CLINVAR | Spectrum and frequencies of BRCA1/2 mutations in Bulgarian high risk breast cancer patients. | 26183948 | 2015 |
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|
A | 0.700 | CausalMutation | CLINVAR | The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study. | 25863477 | 2015 |
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|
A | 0.700 | CausalMutation | CLINVAR | Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer. | 22798144 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | Validation of three BRCA1/2 mutation-carrier probability models Myriad, BRCAPRO and BOADICEA in a population-based series of 183 German families. | 22160602 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | BRCA1 And BRCA2 analysis of Argentinean breastovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin. | 23961350 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. | 21989927 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases. | 22144684 | 2012 |
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|
A | 0.700 | CausalMutation | CLINVAR | BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group. | 9150149 | 1997 |