Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Fanconi anemia: at the crossroads of DNA repair. 21568838

2011
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. 21952622

2011
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Breast cancer risk among male BRCA1 and BRCA2 mutation carriers. 18042939

2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. 16825431

2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Meta-analysis of BRCA1 and BRCA2 penetrance. 17416853

2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR BRCA1 and pancreatic cancer: pedigree findings and their causal relationships. 15796958

2005
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Cancer risks in BRCA2 families: estimates for sites other than breast and ovary. 16141007

2005
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers. 15197194

2004
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. 12677558

2003
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation CLINVAR Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. 9497246

1998