{{Rsnum
|rsid=267608094
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MSH6
|position=47806641
|Gene_s=FBXO11,MSH6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=2
|CLNACC=RCV000035325.2
|CLNALLE=1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.48033780C>T
|CLNSIG=5
|Disease=Lynch syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=FBXO11:80204; MSH6:2956
|GENE_ID=80204; 2956
|GENE_NAME=FBXO11; MSH6
|REF=C
|RSPOS=48033780
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050260000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=267608094
|CLNSRC=InSiGHT
|CLNSRCID=c.3991C>T
}}