{{Rsnum
|rsid=1800932
|Gene=MSH6
|Chromosome=2
|position=47790942
|Orientation=plus
|GMAF=0.1042
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MSH6
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 62.8 | 34.5 | 2.7
| HCB | 100.0 | 0.0 | 0.0
| JPT | 98.2 | 1.8 | 0.0
| YRI | 78.2 | 21.8 | 0.0
| ASW | 82.5 | 15.8 | 1.8
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 88.1 | 11.9 | 0.0
| LWK | 86.4 | 12.7 | 0.9
| MEX | 80.7 | 17.5 | 1.8
| MKK | 84.3 | 15.7 | 0.0
| TSI | 57.8 | 40.2 | 2.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20149637
|Title=Common variants in human CRC genes as low-risk alleles
}}

{{ClinVar
|rsid=1800932
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=48018081
|CHROM=2
|GMAF=0.1044
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050168000000150517100101
|GENEINFO=MSH6:2956
|GENE_NAME=MSH6
|GENE_ID=2956
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.48018081A>G
|CLNSRC=Emory University; InSiGHT
|CLNORIGIN=1
|CLNSIG=2
|CLNDBN=Lynch syndrome; AllHighlyPenetrant
|Disease=Lynch syndrome; AllHighlyPenetrant
|Tags=PM;PMC;SLO;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;PH3;LSD
|CAF=0.8958; 0.1042
|CLNACC=RCV000030265.2; RCV000035321.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; MedGen
|CLNDSDBID=NBK1211:C0009405:315058005; CN169374
|COMMON=1
|CLNSRCID=3109; c.276A>G
}}

{{PMID Auto
|PMID=20386703
|Title=Association between DNA damage response and repair genes and risk of invasive serous ovarian cancer.
|OA=1
}}

{{PMID Auto
|PMID=10537275
|Title=Germ-line msh6 mutations in colorectal cancer families.
}}

{{PMID Auto
|PMID=15805151
|Title=No MSH6 germline mutations in breast cancer families with colorectal and/or endometrial cancer.
|OA=1
}}

{{PMID Auto
|PMID=24357391
|Title=DNA mismatch repair gene MSH6 implicated in determining age at natural menopause
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}