{{Rsnum
|rsid=193922376
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=MSH2
|position=47414421
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922376
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=47641560
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47641560A>T
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Lynch syndrome; not provided
|Disease=Lynch syndrome; not provided
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030256.2; RCV000078424.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|CLNSRCID=c.942+3A>T
}}{{PMID|1071222}} [Microbiological study of a saline soil, El Salitre].

{{PMID|8895729}} Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes.

{{PMID|9311737|OA=1
}} Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

{{PMID|10882759|OA=1
}} Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients.

{{PMID|12658575|OA=1
}} Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.

{{PMID|18270343}} The frequency of Muir-Torre syndrome among Lynch syndrome families.