{{Rsnum
|rsid=1800937
|Gene=MSH6
|Chromosome=2
|position=47798625
|Orientation=plus
|GMAF=0.04959
|Gene_s=MSH6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 75.4 | 21.5 | 3.1
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| 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,T
|CAF=0.9504; 0.04959
|CHROM=2
|CLNACC=RCV000075015.1; RCV000030277.2; RCV000035327.2
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome; AllHighlyPenetrant
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1211:C0009405:315058005; CN169374
|CLNHGVS=NC_000002.11:g.48025764C>A; NC_000002.11:g.48025764C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=InSiGHT; Emory University
|CLNSRCID=c.642C>A; 3120; c.642C>T
|COMMON=1
|Disease=Lynch syndrome; AllHighlyPenetrant
|FwdALT=A,T
|FwdREF=C
|GENEINFO=MSH6:2956
|GENE_ID=2956
|GENE_NAME=MSH6
|REF=C
|RSPOS=48025764
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x050168000000150517100100
|WGT=0
|dbSNPBuildID=89
|rsid=1800937
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}