Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing. 26921362 2016
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. 25186627 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Patterns and functional implications of rare germline variants across 12 cancer types. 26689913 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. 25186627 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. 26315354 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 Biomarker disease CLINGEN FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway. 26637282 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment. 26270727 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland. 25330149 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer. 26315354 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. 25452441 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease. 24556621 2014
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. 24763289 2014
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease. 24556621 2014
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Integrated analysis of germline and somatic variants in ovarian cancer. 24448499 2014
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease CLINVAR Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. 24763289 2014
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 GeneticVariation disease BEFREE Insight into the roles of helicase motif Ia by characterizing Fanconi anemia group J protein (FANCJ) patient mutations. 24573678 2014
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1 		0.760 CausalMutation disease CLINVAR Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas. 24240112 2014