Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 CausalMutation disease CLINVAR Essential Role of BRCA2 in Ovarian Development and Function. 30207912 2018
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease CLINGEN Fanconi anaemia and cancer: an intricate relationship. 29376519 2018
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group. 29661970 2018
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia. 28185119 2017
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GeneticVariation disease BEFREE Fanconi anemia, complementation group D1 with bi-allelic FANCD1 (BRCA2) mutations, is a very rare genetic disorder characterized by early onset of childhood malignancies, including acute leukemia, brain cancer and nephroblastoma. 26657402 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND A novel splice site mutation in the noncoding region of BRCA2: implications for Fanconi anemia and familial breast cancer diagnostics. 24395671 2014
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. 23788249 2013
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GeneticVariation disease UNIPROT A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity. 23108138 2013
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GeneticVariation disease UNIPROT A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay. 21719596 2011
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GeneticVariation disease UNIPROT Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. 16825431 2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GermlineCausalMutation disease ORPHANET Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. 16825431 2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2. 16825431 2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease CLINGEN Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1. 16859999 2006
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease MGD Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1. 16859999 2006
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GermlineCausalMutation disease ORPHANET Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour. 15689453 2005
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GeneticVariation disease UNIPROT Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood. 14670928 2004
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease CLINGEN Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood. 14670928 2004
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GermlineCausalMutation disease ORPHANET Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood. 14670928 2004
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease CLINGEN Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia. 15070707 2004
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease BEFREE The breast cancer susceptibility gene BRCA2 was recently found to be associated with Fanconi anemia complementation group D1 (FA-D1). 14559878 2003
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND Biallelic inactivation of BRCA2 in Fanconi anemia. 12065746 2002
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease CLINGEN Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene. 11861370 2002
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 GeneticVariation disease UNIPROT Biallelic inactivation of BRCA2 in Fanconi anemia. 12065746 2002
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease CLINGEN Biallelic inactivation of BRCA2 in Fanconi anemia. 12065746 2002
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.920 Biomarker disease GENOMICS_ENGLAND