{{Rsnum
|rsid=63750245
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MSH2
|position=47416383
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000030234.2
|CLNALLE=1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47643522C>T
|CLNORIGIN=1
|CLNSIG=5
|Disease=Lynch syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=C
|RSPOS=47643522
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050268000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=63750245
|CLNSRC=InSiGHT
|CLNSRCID=c.1030C>T
}}

{{PMID Auto
|PMID=12655568
|Title=Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in Slovakia.
}}

{{PMID Auto
|PMID=15571801
|Title=Six novel heterozygous MLH1, MSH2, and MSH6 and one homozygous MLH1 germline mutations in hereditary nonpolyposis colorectal cancer.
}}

{{PMID Auto
|PMID=18772310
|Title=Multiplex SNaPshot genotyping for detecting loss of heterozygosity in the mismatch-repair genes MLH1 and MSH2 in microsatellite-unstable tumors.
}}

{{on chip | 23andMe v3}}