Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587778134
rs587778134
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CAA 0.700 CausalMutation CLINVAR Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. 25452441 2015
dbSNP: rs587778134
rs587778134
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CAA 0.700 CausalMutation CLINVAR Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. 26315354 2015