{{Rsnum
|rsid=193922369
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MLH1
|position=37001045
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=63751221
}}{{ClinVar
|rsid=193922369
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37042536
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=050268400711000002100100
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.37042536C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Hereditary non-polyposis colon cancer
|Disease=Hereditary non-polyposis colon cancer
|Tags=PM;PMC;S3D;NSN;REF;SYN;U5;OTH;OTHERKG;LSD
}}{{PMID Auto
|PMID=17312
|Title=[Gerontology in rural and mountains regions aged people in the country and in mountain regions (author's transl)].
}}

{{PMID Auto
|PMID=10480359
|Title=Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer.
}}

{{PMID Auto
|PMID=14512394
|Title=Altered expression of MLH1, MSH2, and MSH6 in predisposition to hereditary nonpolyposis colorectal cancer.
}}

{{PMID Auto
|PMID=15235038
|Title=Novel splicing associations of hereditary colon cancer related DNA mismatch repair gene mutations.
|OA=1
}}

{{PMID Auto
|PMID=15872200
|Title=Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
}}

{{PMID Auto
|PMID=18415027
|Title=Genome-wide copy neutral LOH is infrequent in familial and sporadic microsatellite unstable carcinomas.
}}