Gene: BRCA2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 GeneticVariation phenotype CLINVAR Mutations in BRCA2 and PALB2 in male breast cancer cases from the United States. 20927582 2011
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503deITT mutation previously found to recur in different ethnic populations. 11359068 2001
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR BRCA1 and BRCA2 mutations in women with familial or early-onset breast/ovarian cancer in the Czech Republic. 15024741 2004
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 GeneticVariation phenotype CLINVAR Multiple sequence variants of BRCA2 exon 7 alter splicing regulation. 22962691 2012
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. 8589730 1996
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer. 20694749 2011
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Significant clinical impact of recurrent BRCA1 and BRCA2 mutations in Mexico. 25236687 2015
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR BRCA1 and BRCA2 mutations in an Asian clinic-based population detected using a comprehensive strategy. 18006916 2008
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma. 17624602 2008
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 GeneticVariation phenotype CLINVAR BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative research. 18704680 2009
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 GeneticVariation phenotype CLINVAR Two mutations of BRCA2 gene at exon and splicing site in a woman who underwent oncogenetic counseling. 19179552 2009
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 GeneticVariation phenotype CLINVAR Adding In Silico Assessment of Potential Splice Aberration to the Integrated Evaluation of BRCA Gene Unclassified Variants. 26913838 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR The P1812A and P25T BRCA1 and the 5164del4 BRCA2 mutations: occurrence in high-risk non-Ashkenazi Jews. 17020472 2007
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR BRCA1 and BRCA2 mutations in a study of African American breast cancer patients. 15533909 2005
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Biallelic inactivation of BRCA2 in Fanconi anemia. 12065746 2002
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR BRCA1-2 mutations in breast cancer: identification of nine new variants of BRCA1-2 genes in a population from central Western Spain. 15876480 2006
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype 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 		0.600 CausalMutation phenotype CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2017
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol. 26787237 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Inherited predisposition to breast cancer among African American women. 25428789 2015
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR BRCA1, BRCA2 and TP53 mutations in very early-onset breast cancer with associated risks to relatives. 16644204 2006
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 Biomarker phenotype CLINGEN Transformation of the fallopian tube secretory epithelium leads to high-grade serous ovarian cancer in Brca;Tp53;Pten models. 24332043 2013
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes. 21735045 2012
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 CausalMutation phenotype CLINVAR Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes. 22703879 2012
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2 		0.600 GeneticVariation phenotype CLINVAR Genetic diagnosis of familial breast cancer using clonal sequencing. 20127978 2010