{{Rsnum
|rsid=267608049
|Chromosome=2
|Orientation=plus
|geno1=(AG;AG)
|geno2=(AG;TC)
|geno3=(TC;TC)
|Gene=MSH6
|position=47799597
|Gene_s=MSH6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AAG
|CHROM=2
|CLNACC=RCV000074669.1
|CLNALLE=1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000002.11:g.48026736_48026737delTCinsAG
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.1614_1615delinsAG
|Disease=Lynch syndrome
|FwdALT=AG
|FwdREF=TC
|GENEINFO=MSH6:2956
|GENE_ID=2956
|GENE_NAME=MSH6
|REF=ATC
|RSPOS=48026735
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=MNV
|VP=0x050260000000000002100800
|WGT=0
|dbSNPBuildID=137
|rsid=267608049
}}