{{Rsnum
|rsid=121912965
|Chromosome=3
|Orientation=plus
|geno1=(AC;AC)
|geno2=(AC;TG)
|geno3=(TG;TG)
|Gene=MLH1
|position=36993651
|Gene_s=EPM2AIP1,MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120436
|rsnum=121912965
|variant=0028
}}{{ClinVar
|rsid=121912965
|Reversed=0
|FwdREF=TG
|FwdALT=AC
|REF=ATG
|ALT=AAC
|RSPOS=37035141
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110800
|GENEINFO=EPM2AIP1:9852; MLH1:4292
|GENE_NAME=EPM2AIP1; MLH1
|GENE_ID=9852; 4292
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.37035142_37035143delTGinsAC
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120436.0028
|CLNSIG=5
|CLNCUI=C0265325; C1333991
|CLNDBN=Turcot syndrome; Lynch syndrome II; Lynch syndrome
|Disease=Turcot syndrome; Lynch syndrome II; Lynch syndrome
|CLNACC=RCV000018639.26; RCV000018640.26; RCV000075101.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0265325:276300:252202:61665008; NBK1211:C1333991:609310:144; NBK1211:C0009405:315058005
}}