Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs775537066
rs775537066
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0006142
Disease:
Malignant neoplasm of breast
CA 0.700 CausalMutation CLINVAR Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer. 29922827 2018
dbSNP: rs775537066
rs775537066
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0006142
Disease:
Malignant neoplasm of breast
CA 0.700 CausalMutation CLINVAR No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. 26921362 2016
dbSNP: rs775537066
rs775537066
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0006142
Disease:
Malignant neoplasm of breast
CA 0.700 CausalMutation CLINVAR Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. 26315354 2015
dbSNP: rs775537066
rs775537066
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0006142
Disease:
Malignant neoplasm of breast
CA 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311 2011
dbSNP: rs775537066
rs775537066
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0006142
Disease:
Malignant neoplasm of breast
CA 0.700 CausalMutation CLINVAR Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. 17033622 2006