{{Rsnum
|rsid=63750006
|Gene=MSH2
|Chromosome=2
|position=47429920
|Orientation=plus
|GMAF=0.001837
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ClinVar
|ALT=A,T
|CAF=0.9982; 0.001837; .
|CHROM=2
|CLNACC=RCV000076079.1; RCV000076080.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47657059C>A; NC_000002.11:g.47657059C>T
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.1255C>A; c.1255C>T
|COMMON=1
|Disease=Lynch syndrome
|FwdALT=A,T
|FwdREF=C
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=C
|RSPOS=47657059
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050260000000000016100100
|WGT=0
|dbSNPBuildID=137
|rsid=63750006
}}