×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Recent progress in Lynch syndrome and other familial colorectal cancer syndromes.
29485237
2018
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens.
28176205
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Prevalence of pathogenic germline variants detected by multigene sequencing in unselected Japanese patients with ovarian cancer.
29348823
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
28944238
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
28514183
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2.
28466842
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Longitudinal analysis of treatment-induced genomic alterations in gliomas.
28153049
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6.
28528517
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.
28944238
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
27696107
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
28449805
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
28531214
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
28874130
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
In Silico Systems Biology Analysis of Variants of Uncertain Significance in Lynch Syndrome Supports the Prioritization of Functional Molecular Validation.
28765196
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
A rare case of choroid plexus carcinoma that led to the diagnosis of Lynch syndrome (hereditary nonpolyposis colorectal cancer).
28460341
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
28874130
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort.
29212164
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing.
28502729
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.
28481244
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
GeneticVariation
CLINVAR
Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.
28481244
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series.
28283864
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
28135145
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
28195393
2017
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
Neoplastic Syndromes, Hereditary
0.110
CausalMutation
CLINVAR
Assigning clinical meaning to somatic and germ-line whole-exome sequencing data in a prospective cancer precision medicine study.
28125075
2017