rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
23535968
2013
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.
23408351
2013
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
25452455
2015
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
25394175
2015
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
25003300
2014
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
25645574
2015
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
20065170
2010
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
25070057
2014
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Lynch Syndrome: A Primer for Urologists and Panel Recommendations.
25711197
2015
rs28929484
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
24493721
2014
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system.
18781619
2008
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer.
10375096
1999
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects.
18561205
2008
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
G
0.800
GeneticVariation
CLINVAR
Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants.
26951660
2016
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Identification of individuals at risk for Lynch syndrome using targeted evaluations and genetic testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer joint practice guideline.
22167527
2012
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Population-based molecular detection of hereditary nonpolyposis colorectal cancer.
10829038
2000
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
27854360
2017
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
G
0.800
CausalMutation
CLINVAR
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.
15870828
2005
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Hereditary colorectal cancer syndromes: American Society of Clinical Oncology Clinical Practice Guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology Clinical Practice Guidelines.
25452455
2015
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
G
0.800
GeneticVariation
CLINVAR
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
24362816
2014
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer.
25003300
2014
rs587779067
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.800
GeneticVariation
UNIPROT
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
25356965
2015