| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
C | 0.700 | CausalMutation | CLINVAR | Novel germline mutations and unclassified variants of BRCA1 and BRCA2 genes in Chinese women with familial breast/ovarian cancer. | 26852015 | 2016 |
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|
C | 0.700 | CausalMutation | CLINVAR | Prevalence and spectrum of BRCA germline variants in mainland Chinese familial breast and ovarian cancer patients. | 26848529 | 2016 |
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|
C | 0.700 | CausalMutation | CLINVAR | Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer. | 26824983 | 2016 |
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|
C | 0.700 | CausalMutation | CLINVAR | Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. | 27257965 | 2016 |
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|
C | 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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|
C | 0.700 | CausalMutation | CLINVAR | One Case of a BRCA1 Germ Line Mutation Ovarian Carcinoma Patient Based on Abnormal Immunohistochemistry Finding. | 25366075 | 2014 |
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|
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 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations. | 16455195 | 2007 |
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|
C | 0.700 | CausalMutation | CLINVAR | A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting. | 16683254 | 2006 |
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|
C | 0.700 | CausalMutation | CLINVAR | Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients. | 15117986 | 2004 |
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|
C | 0.700 | CausalMutation | CLINVAR | A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families. | 8554067 | 1996 |