{{Rsnum
|rsid=63751108
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MSH2
|position=47429881
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSH2
}}{{omim
|id=609309
|rsnum=63751108
|variant=0003
}}{{ClinVar
|rsid=63751108
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=47657020
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=MSH2:4436
|GENE_NAME=MSH2
|GENE_ID=4436
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47657020C>T
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.1216C>T; 609309.0003
|CLNSIG=5
|CLNCUI=C2936783
|CLNDBN=Lynch syndrome I; Lynch syndrome
|Disease=Lynch syndrome I; Lynch syndrome
|CLNACC=RCV000001825.1; RCV000030238.2
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C2936783:120435:144; NBK1211:C0009405:315058005
}}{{PMID Auto
|PMID=1573177
|Title=Long-term follow-up of Morton's neuroma.
}}

{{PMID Auto
|PMID=8062247
|Title=hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
}}

{{PMID Auto
|PMID=9288790
|Title=Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees.
}}

{{PMID Auto
|PMID=12362047
|Title=Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States.
|OA=1
}}

{{PMID Auto
|PMID=17414604
|Title=Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.
|OA=1
}}

{{PMID Auto
|PMID=19459153
|Title=High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.
}}