{{Rsnum
|rsid=193922370
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MLH1
|position=37008813
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922370
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=37050304
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100104
|WGT=0
|VC=SNV
|CLNALLE=1; 3
|CLNHGVS=NC_000003.11:g.37050304G>A; NC_000003.11:g.37050304G>T
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Lynch syndrome
|Disease=Lynch syndrome
|Tags=PM;PMC;OTHERKG;LSD;NOV
|CLNACC=RCV000030226.2; RCV000075720.1
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|GENEINFO=MLH1:4292
|GENE_ID=4292
|GENE_NAME=MLH1
|CLNSRCID=c.454-1G>A; c.454-1G>T
}}{{PMID|7584997}} Founding mutations and Alu-mediated recombination in hereditary colon cancer.