Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry. 27741520 2016
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol. 26787237 2016
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer. 25479140 2015
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases. 22144684 2012
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancer. 22866093 2011
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Expression of cancer testis antigens in human BRCA-associated breast cancers: potential targets for immunoprevention? 21465317 2011
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Case report: de novo BRCA2 gene mutation in a 35-year-old woman with breast cancer. 19796187 2009
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting. 16683254 2006
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Cancer variation associated with the position of the mutation in the BRCA2 gene. 15131399 2004
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in women from Shanghai China. 14973102 2004
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Shared genetic susceptibility to breast cancer, brain tumors, and Fanconi anemia. 14559878 2003
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Contribution of BRCA1 and BRCA2 mutations to breast and ovarian cancer in Pakistan. 12181777 2002
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. 11179017 2001
dbSNP: rs80359479
rs80359479
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0677776
Disease:
Hereditary Breast and Ovarian Cancer Syndrome
CA 0.700 CausalMutation CLINVAR The breast cancer information core: database design, structure, and scope. 10923033 2000