{{Rsnum
|rsid=121912962
|Chromosome=3
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AAG)
|geno3=(AAG;AAG)
|Gene=MLH1
|position=37047633
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120436
|rsnum=121912962
|variant=0018
}}{{ClinVar
|rsid=121912962
|Reversed=0
|FwdREF=AAG
|FwdALT=
|REF=GAAG
|ALT=G
|RSPOS=37089123
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=MLH1:4292
|GENE_NAME=MLH1
|GENE_ID=4292
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.37089124_37089126delAAG
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120436.0018
|CLNSIG=5
|CLNCUI=C1333991; C1333991
|CLNDBN=Lynch syndrome II
|Disease=Lynch syndrome II
|CLNACC=RCV000018627.26
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1211:C1333991:609310:144
}}