{{Rsnum
|rsid=138705565
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MLH1
|position=36993627
|Gene_s=EPM2AIP1,MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=138705565
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=37035118
|CHROM=3
|dbSNPBuildID=134
|SSR=0
|SAO=1
|VP=0x050260000000000002100100
|GENEINFO=EPM2AIP1:9852; MLH1:4292
|GENE_NAME=EPM2AIP1; MLH1
|GENE_ID=9852; 4292
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000003.11:g.37035118G>C
|CLNSRC=InSiGHT
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Lynch syndrome
|Disease=Lynch syndrome
|Tags=PM;S3D;OTHERKG;LSD
|CLNACC=RCV000030232.2
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNSRCID=c.80G>C
}}