{{Rsnum
|rsid=63750329
|Chromosome=2
|Orientation=plus
|geno1=(AGTG;AGTG)
|geno2=(AGTG;TT)
|geno3=(TT;TT)
|Gene=MSH2
|position=47412531
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TTT
|CHROM=2
|CLNACC=RCV000076705.1
|CLNALLE=1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47639670_47639673delAGTGinsTT
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.763_766delinsTT
|Disease=Lynch syndrome
|FwdALT=TT
|FwdREF=AGTG
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=TAGTG
|RSPOS=47639669
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=DIV
|VP=0x050260000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=63750329
}}