Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 GeneticVariation CLINVAR A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques. 15951958 2005
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 GeneticVariation CLINVAR Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer. 11504767 2001
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 GeneticVariation CLINVAR Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers. 10615237 1999
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 GeneticVariation CLINVAR Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. 9585613 1998
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 GeneticVariation CLINVAR BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease. 9537231 1998
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 GeneticVariation CLINVAR Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. 9150154 1997
dbSNP: rs80359436
rs80359436
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C2675520
Disease:
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
A 0.700 CausalMutation CLINVAR