{{Rsnum
|rsid=28929484
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MSH2
|position=47475180
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000001826.1; RCV000030246.2
|CLNALLE=1
|CLNDBN=Lynch syndrome I; Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C2936783:120435:144; NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47702319C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNSRCID=c.1915C>T; 609309.0004
|Disease=Lynch syndrome I; Lynch syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=C
|RSPOS=47702319
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=28929484
}}{{PMID Auto
|PMID=8062247
|Title=hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
}}

{{PMID Auto
|PMID=8261515
|Title=Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
}}

{{PMID Auto
|PMID=9630599
|Title=Functional genetic tests of DNA mismatch repair protein activity in Saccharomyces cerevisiae.
}}

{{PMID Auto
|PMID=9718327
|Title=Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
|OA=1
}}

{{PMID Auto
|PMID=14518068
|Title=Molecular dimensions of gastrointestinal tumors: some thoughts for digestion.
}}

{{PMID Auto
|PMID=16395668
|Title=Systematic mRNA analysis for the effect of MLH1 and MSH2 missense and silent mutations on aberrant splicing.
}}