| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
G | 0.700 | CausalMutation | CLINVAR | Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women. | 27836010 | 2016 |
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|
G | 0.700 | CausalMutation | CLINVAR | Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing. | 25366421 | 2015 |
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|
G | 0.700 | CausalMutation | CLINVAR | Recurrent mutations of BRCA1 and BRCA2 in Poland: an update. | 24528374 | 2015 |
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|
G | 0.700 | CausalMutation | CLINVAR | Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast Cancers. | 26083025 | 2015 |
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|
G | 0.700 | CausalMutation | CLINVAR | High prevalence of BRCA1 founder mutations in Greek breast/ovarian families. | 24010542 | 2014 |
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|
G | 0.700 | CausalMutation | CLINVAR | Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management. | 22535016 | 2012 |
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|
G | 0.700 | CausalMutation | CLINVAR | Prevalence of the most frequent BRCA1 mutations in Polish population. | 21503673 | 2011 |
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|
G | 0.700 | CausalMutation | CLINVAR | Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. | 21324516 | 2011 |
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|
G | 0.700 | CausalMutation | CLINVAR | BRCA1 and BRCA2 mutations in Turkish breast/ovarian families and young breast cancer patients. | 10952777 | 2000 |
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|
G | 0.700 | CausalMutation | CLINVAR | Mutation analysis of the BRCA1 gene in ovarian cancers. | 7606717 | 1995 |