{{Rsnum
|rsid=63751656
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MSH2
|position=47466807
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C,G,T
|CHROM=2
|CLNACC=RCV000076213.1; RCV000076214.1; RCV000076215.1
|CLNALLE=1; 2; 3
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47693946A>C; NC_000002.11:g.47693946A>G; NC_000002.11:g.47693946A>T
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.1660A>C; c.1660A>G; c.1660A>T
|Disease=Lynch syndrome
|FwdALT=C,G,T
|FwdREF=A
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=A
|RSPOS=47693946
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;NOV
|VC=SNV
|VP=0x050260000000000002100104
|WGT=0
|dbSNPBuildID=137
|rsid=63751656
}}