{{Rsnum
|rsid=12476364
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MSH2
|position=47416295
|Gene_s=MSH2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{ClinVar
|ALT=A,C
|CHROM=2
|CLNACC=RCV000076757.1; RCV000076758.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.47643434G>A; NC_000002.11:g.47643434G>C
|CLNSIG=4
|CLNSRC=InSiGHT
|CLNSRCID=c.943-1G>A; c.943-1G>C
|Disease=Lynch syndrome
|FwdALT=A,C
|FwdREF=G
|GENEINFO=MSH2:4436
|GENE_ID=4436
|GENE_NAME=MSH2
|REF=G
|RSPOS=47643434
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;HD;GNO;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x050068000000000503100100
|WGT=0
|dbSNPBuildID=120
|rsid=12476364
}}

{{on chip | HumanOmni1Quad}}