Source: CLINVAR ×
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
T | 0.700 | CausalMutation | CLINVAR | Detection of BRCA1 and BRCA2 germline mutations in Japanese population using next-generation sequencing. | 25802882 | 2015 |
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|
T | 0.700 | CausalMutation | CLINVAR | Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes. | 21735045 | 2012 |
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|
T | 0.700 | CausalMutation | CLINVAR | The Korean Hereditary Breast Cancer (KOHBRA) study: protocols and interim report. | 21497495 | 2011 |
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|
T | 0.700 | CausalMutation | CLINVAR | Breast cancer in young women (YBC): prevalence of BRCA1/2 mutations and risk of secondary malignancies across diverse racial groups. | 19491284 | 2009 |
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|
T | 0.700 | CausalMutation | CLINVAR | Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer. | 17100994 | 2006 |
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|
T | 0.700 | CausalMutation | CLINVAR | BRCA2 mutations in 154 finnish male breast cancer patients. | 15548363 | 2005 |
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|
T | 0.700 | CausalMutation | CLINVAR | Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients. | 15117986 | 2004 |
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|
T | 0.700 | CausalMutation | CLINVAR | Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes. | 9361038 | 1997 |