{{Rsnum
|rsid=63749811
|Chromosome=2
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=MSH2
|position=47476474
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=63749811
|Reversed=0
|FwdREF=G
|FwdALT=
|REF=TG
|ALT=T
|RSPOS=47703612
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100200
|GENEINFO=MSH2:4436
|GENE_NAME=MSH2
|GENE_ID=4436
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47703613delG
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Lynch syndrome I; Lynch syndrome
|Disease=Lynch syndrome I; Lynch syndrome
|Tags=PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000001830.1; RCV000030250.2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C2936783:120435:144; NBK1211:C0009405:315058005
|CLNSRCID=c.2113del; 609309.0008
}}

{{PMID Auto
|PMID=8872463
|Title=Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer.
}}

{{PMID Auto
|PMID=10080150
|Title=Reduction in hMSH2 mRNA levels by premature translation termination: implications for mutation screening in hereditary nonpolyposis colorectal cancer.
}}

{{PMID Auto
|PMID=16142001
|Title=Value of microsatellite instability typing in detecting hereditary non-polyposis colorectal cancer. A prospective multicentric study by the Association Aquitaine Gastro.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}