{{Rsnum
|rsid=63750583
|Chromosome=2
|Orientation=plus
|geno1=(CT;CT)
|geno2=(CT;GC)
|geno3=(GC;GC)
|Gene=MSH2
|position=47463120
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TCT
|CHROM=2
|CLNACC=RCV000076172.1
|CLNALLE=1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47690259_47690260delGCinsCT
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.1476_1477delinsCT
|Disease=Lynch syndrome
|FwdALT=CT
|FwdREF=GC
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=TGC
|RSPOS=47690258
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=MNV
|VP=0x050260000000000002100800
|WGT=0
|dbSNPBuildID=137
|rsid=63750583
}}