{{Rsnum
|rsid=63750781
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MLH1
|position=37004444
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G,T
|CHROM=3
|CLNACC=RCV000075665.1; RCV000018626.22; RCV000075666.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome; Lynch syndrome II
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1211:C0009405:315058005; NBK1211:C1333991:609310:144
|CLNHGVS=NC_000003.11:g.37045935C>G; NC_000003.11:g.37045935C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNSRCID=c.350C>G; c.350C>T; 120436.0017
|Disease=Lynch syndrome; Lynch syndrome II
|FwdALT=G,T
|FwdREF=C
|GENEINFO=MLH1:4292
|GENE_ID=4292
|GENE_NAME=MLH1
|REF=C
|RSPOS=37045935
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=63750781
}}