Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian study. 27062684 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease 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
0.700 CausalMutation disease CLINVAR Genetic testing in a cohort of young patients with HER2-amplified breast cancer. 26681682 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Exonic Splicing Mutations Are More Prevalent than Currently Estimated and Can Be Predicted by Using In Silico Tools. 26761715 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers. 26586665 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR In silico, in vitro and case-control analyses as an effective combination for analyzing BRCA1 and BRCA2 unclassified variants in a population-based sample. 27886673 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries. 26187060 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR BRCA1 and BRCA2 mutations in Japanese patients with ovarian, fallopian tube, and primary peritoneal cancer. 26439132 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 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: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients. 26483394 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol. 26787237 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing. 26757417 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries. 26187060 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G>A/c.7008-2A>T genotype Response to: Nagy PL, Mansukhani M. The role of clinical genomic testing in diagnosis and discovery of pathogenic mutations. Expert Rev Mol Diagn 2015;15(9):1101-5. 27125725 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Prevalence of Hispanic BRCA1 and BRCA2 mutations among hereditary breast and ovarian cancer patients from Brazil reveals differences among Latin American populations. 27425403 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 GeneticVariation disease CLINVAR Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA. 26556299 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer. 27153395 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR A Survey of BRCA1, BRCA2, and PALB2 mutations in women with breast cancer in Trinidad and Tobago. 27469594 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients. 26541979 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients. 27406733 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease 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
0.700 CausalMutation disease CLINVAR Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel. 27157322 2016
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.700 CausalMutation disease CLINVAR Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2. 26360800 2016