{{Rsnum
|rsid=193922374
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MSH2
|position=47410148
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922374
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=47637287
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050260000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.47637287A>G
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Lynch syndrome
|Disease=Lynch syndrome
|Tags=PM;S3D;OTHERKG;LSD
|CLNACC=RCV000030254.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|CLNSRCID=c.421A>G
}}