{{Rsnum
|rsid=111052004
|Chromosome=3
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MLH1
|position=36993549
|Gene_s=EPM2AIP1,MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,G
|CHROM=3
|CLNACC=RCV000075620.1; RCV000075622.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000003.11:g.37035040T>A; NC_000003.11:g.37035040T>G
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.2T>A; c.2T>G
|Disease=Lynch syndrome
|FwdALT=A,G
|FwdREF=T
|GENEINFO=EPM2AIP1:9852; MLH1:4292
|GENE_ID=9852; 4292
|GENE_NAME=EPM2AIP1; MLH1
|REF=T
|RSPOS=37035040
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD
|VC=SNV
|VP=0x050260000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=111052004
}}