{{Rsnum
|rsid = 28929483
|Gene = MSH2
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=2
|position=47475130
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSH2
}}{{omim
|desc=COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 1
|id=609309
|rsnum=28929483
|variant=0001
}}{{ClinVar
|rsid=28929483
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=47702269
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MSH2:4436
|GENE_NAME=MSH2
|GENE_ID=4436
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47702269C>T
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.1865C>T; 609309.0001
|CLNSIG=5
|CLNCUI=C2936783
|CLNDBN=Lynch syndrome I; Lynch syndrome
|Disease=Lynch syndrome I; Lynch syndrome
|CLNACC=RCV000001823.1; RCV000076307.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C2936783:120435:144; NBK1211:C0009405:315058005
}}