{{Rsnum
|rsid=281864942
|Chromosome=2
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GG)
|geno3=(GG;GG)
|Gene=MSH2
|position=47403378
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSH2
}}{{ClinVar
|ALT=AG,AGG
|CHROM=2
|CLNACC=RCV000076308.1; RCV000076311.1
|CLNALLE=2; 1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47630516_47630517dupGG; NC_000002.11:g.47630517dupG
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.186_187dup; c.187dup
|Disease=Lynch syndrome
|FwdALT=AG,AGG
|FwdREF=A
|REF=A
|RSPOS=47630512
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=DIV
|VP=0x050260000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=281864942
}}