×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
GeneticVariation
disease
CLINVAR
Microsatellite Instability Is Associated With the Presence of Lynch Syndrome Pan-Cancer.
30376427
2019
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Outcomes of disease-specific next-generation sequencing gene panel testing in adolescents and young adults with colorectal cancer.
31101557
2019
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.
28932927
2018
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.
29575718
2018
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
GeneticVariation
disease
CLINVAR
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
28152038
2017
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
27978560
2017
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Thyroid cancer in a patient with Lynch syndrome - case report and literature review.
28769567
2017
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.
28449805
2017
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
GeneticVariation
disease
CLINVAR
Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
28514183
2017
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.
27606285
2016
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Frequent mismatch-repair defects link prostate cancer to Lynch syndrome.
27013479
2016
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
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:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.
26951660
2016
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
27064304
2016
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.
25559809
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers.
25110875
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Genetic features of Lynch syndrome in the Israeli population.
25430799
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
GeneticVariation
disease
CLINVAR
Genetic features of Lynch syndrome in the Israeli population.
25430799
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case.
25173403
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
GeneticVariation
disease
CLINVAR
Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
25980754
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.
26437257
2015
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Lynch Syndrome in patients with clear cell and endometrioid cancers of the ovary.
25093288
2014
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Muir-Torre syndrome: case report and molecular characterization.
24474082
2014
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
1.000
CausalMutation
disease
CLINVAR
Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
25194673
2014