{{Rsnum
|rsid = 28930073
|Gene = MLH1
|geno1 = (C;C)
|geno2 = (C;G)
|geno3 = (G;G)
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|Chromosome=3
|position=37007004
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
| id = 120436
| variant = 0019
| desc    = COLORECTAL CANCER, SPORADIC, SUSCEPTIBILITY TO
| rsnum   = 28930073
}}
{{PMID Auto
|PMID=19665066
|Title=A MLH1 polymorphism that increases cancer risk is associated with better outcome in sporadic colorectal cancer
}}{{ClinVar
|ALT=C
|CHROM=3
|CLNACC=RCV000018628.1; RCV000075697.1
|CLNALLE=1
|CLNDBN=Colorectal cancer, sporadic, susceptibility to; Lynch syndrome
|CLNHGVS=NC_000003.11:g.37048495G>C
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNSRCID=c.394G>C; 120436.0019
|Disease=Colorectal cancer; Lynch syndrome
|FwdALT=C
|FwdREF=G
|GENEINFO=MLH1:4292
|GENE_ID=4292
|GENE_NAME=MLH1
|REF=G
|RSPOS=37048495
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=28930073
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
}}