Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer. 29368341 2018
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Pathogenic Germline Variants in 10,389 Adult Cancers. 29625052 2018
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Genetic variants in ATM, H2AFX and MRE11 genes and susceptibility to breast cancer in the polish population. 29678143 2018
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Development of a high risk pancreatic screening clinic using 3.0 T MRI. 29101607 2018
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Deleterious Germline Mutations in Patients With Apparently Sporadic Pancreatic Adenocarcinoma. 28767289 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Molecular and Functional Characterization of a Cohort of Spanish Patients with Ataxia-Telangiectasia. 27664052 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. 28195393 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results. 28008555 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels. 28152038 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer. 27978560 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks. 28779002 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Multigene panels in Ashkenazi Jewish patients yield high rates of actionable mutations in multiple non-BRCA cancer-associated genes. 28495237 2017
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias. 27528516 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group 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: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer. 27433846 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Allogeneic-matched sibling stem cell transplantation in a 13-year-old boy with ataxia telangiectasia and EBV-positive non-Hodgkin lymphoma. 27159176 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings. 27083775 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 GeneticVariation group CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Ataxia Telangiectasia Masquerading as Hyper IgM Syndrome. 26220245 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Novel ATM mutations with ataxia-telangiectasia. 26628246 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients. 26822949 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations. 27449771 2016
Entrez Id: 160140
Gene Symbol: C11orf65
C11orf65
0.100 CausalMutation group CLINVAR Targeted next-generation sequencing in chronic lymphocytic leukemia: a high-throughput yet tailored approach will facilitate implementation in a clinical setting. 25480502 2015