Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
C | 0.700 | CausalMutation | CLINVAR | Mutations in context: implications of BRCA testing in diverse populations. | 28918466 | 2018 |
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C | 0.700 | CausalMutation | CLINVAR | Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. | 26681312 | 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 | Massively Parallel Functional Analysis of BRCA1 RING Domain Variants. | 25823446 | 2015 |
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|
C | 0.700 | CausalMutation | CLINVAR | Seventeen years after BRCA1: what is the BRCA mutation status of the breast cancer patients in Africa? - a systematic review. | 23519070 | 2012 |
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|
C | 0.700 | CausalMutation | CLINVAR | Recurrent BRCA1 and BRCA2 mutations in breast cancer patients of African ancestry. | 22739995 | 2012 |
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|
C | 0.700 | CausalMutation | CLINVAR | High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients. | 22034289 | 2012 |
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|
C | 0.700 | CausalMutation | CLINVAR | Evidence for an ancient BRCA1 mutation in breast cancer patients of Yoruban ancestry. | 18679828 | 2009 |
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|
C | 0.700 | CausalMutation | CLINVAR | High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. | 17591842 | 2007 |
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|
C | 0.700 | CausalMutation | CLINVAR | BRCA1 genetic testing in 106 breast and ovarian cancer families from Southern Italy (Sicily): a mutation analyses. | 17221156 | 2007 |