Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas. 8968085

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR BRCA2 germline mutations in male breast cancer cases and breast cancer families. 8673091

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Identification of the breast cancer susceptibility gene BRCA2. 8524414

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR BRCA2 mutations in primary breast and ovarian cancers. 8640235

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Somatic and germline mutations of the BRCA2 gene in sporadic ovarian cancer. 8705994

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. 8589730

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. 8673090

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. 8673089

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Mutations of the BRCA2 gene in ovarian carcinomas. 8665505

1996

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR BRCA2 mutations in hereditary breast and ovarian cancer in France. 9150172

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR BRCA1 and BRCA2 mutation analysis in 86 early onset breast/ovarian cancer patients. 9429140

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. 8988179

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR A low proportion of BRCA2 mutations in Finnish breast cancer families. 9150152

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population. 9012404

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes? 9042907

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Breast Cancer Linkage Consortium. 9167459

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Analysis of BRCA1 and BRCA2 mutations in Hungarian families with breast or breast-ovarian cancer. 9150174

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes. 9361038

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. 9150154

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Study of a single BRCA2 mutation with high carrier frequency in a small population. 9150155

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR BRCA2 germline mutations in Japanese breast cancer families. 9133456

1997

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families. 9792861

1998

Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation 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
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.130 CausalMutation CLINVAR Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk. 9667259

1998