{{Rsnum
|rsid=267608019
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MSH2
|position=47480872
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=2
|CLNACC=RCV000076518.1; RCV000076519.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47708011G>A; NC_000002.11:g.47708011G>T
|CLNSIG=4
|CLNSRC=InSiGHT
|CLNSRCID=c.2634+1G>A; c.2634+1G>T
|Disease=Lynch syndrome
|FwdALT=A,T
|FwdREF=G
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=G
|RSPOS=47708011
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=267608019
}}