{{Rsnum
|rsid=4647269
|Gene=MLH1
|Chromosome=3
|position=37016100
|Orientation=plus
|GMAF=0.2975
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.0 | 49.6 | 27.4
| HCB | 86.1 | 13.9 | 0.0
| JPT | 68.1 | 29.2 | 2.7
| YRI | 61.9 | 32.0 | 6.1
| ASW | 43.9 | 47.4 | 8.8
| CHB | 86.1 | 13.9 | 0.0
| CHD | 89.8 | 10.2 | 0.0
| GIH | 60.4 | 33.7 | 5.9
| LWK | 63.6 | 30.9 | 5.5
| MEX | 43.1 | 48.3 | 8.6
| MKK | 85.3 | 14.1 | 0.6
| TSI | 32.4 | 48.0 | 19.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=22594646
|Title=Common variants in mismatch repair genes associated with increased risk of sperm DNA damage and male infertility
|OA=1
}}

{{PMID Auto
|PMID=19930554
|Title=Partial loss of heterozygosity events at the mutated gene in tumors from MLH1/MSH2 large genomic rearrangement carriers.
|OA=1
}}

{{ClinVar
|ALT=T
|CAF=0.7025; 0.2975
|CHROM=3
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.37057591C>T
|CLNSIG=2
|COMMON=1
|FwdALT=T
|FwdREF=C
|GENEINFO=MLH1:4292
|GENE_ID=4292
|GENE_NAME=MLH1
|REF=C
|RSPOS=37057591
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x05016800000017051f100100
|WGT=0
|dbSNPBuildID=111
|rsid=4647269
|CLNACC=RCV000075859.1
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNSRC=InSiGHT
|CLNSRCID=c.791-1406C>T
|Disease=Lynch syndrome
}}

{{on chip | Affy GenomeWide 6}}