{{Rsnum
|rsid=41294988
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MSH6
|position=47783271
|Gene_s=MSH6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=41294988
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=48010410
|CHROM=2
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|GENEINFO=MSH6:2956
|GENE_NAME=MSH6
|GENE_ID=2956
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.48010410A>C
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Lynch syndrome
|Disease=Lynch syndrome
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030274.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNSRCID=c.38A>C
}}

{{PMID Auto
|PMID=19389263
|Title=Investigation on the role of nsSNPs in HNPCC genes--a bioinformatics approach.
|OA=1
}}

{{PMID Auto
|PMID=18033691
|Title=Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer.
}}

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