Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. 9585613 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. 9585613 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. 9667259 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 Biomarker disease CLINGEN Stable interaction between the products of the BRCA1 and BRCA2 tumor suppressor genes in mitotic and meiotic cells. 9774970 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease. 9537231 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families. 9792861 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. 9667259 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Characterization of ten novel and 13 recurring BRCA1 and BRCA2 germline mutations in Italian breast and/or ovarian carcinoma patients. Mutations in brief no. 178. Online. 10660329 1998
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes. 10486320 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Cancer risks in BRCA2 mutation carriers. 10433620 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G. 10595255 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Survival in hereditary breast cancer associated with germline mutations of BRCA2. 10550133 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Truncated BRCA2 is cytoplasmic: implications for cancer-linked mutations. 10570174 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations. 10644434 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR BRCA1/BRCA2 germline mutations in locally recurrent breast cancer patients after lumpectomy and radiation therapy: implications for breast-conserving management in patients with BRCA1/BRCA2 mutations. 10506595 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2. 10188893 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers. 10615237 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study. 10498392 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects. 10227398 1999
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR The BRCA2 genetic variant IVS7 + 2T-->G is a mutation. 11185744 2000
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families. 10638982 2000
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families. 10638982 2000
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR 2157delG: a frequent mutation in BRCA2 missed by PTT. 11106360 2000
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR BRCA2 germline mutations among early onset breast cancer patients unselected for family history of the disease. 10978364 2000
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer. 10807692 2000