{{Rsnum
|rsid=35001569
|Gene=MLH1
|Chromosome=3
|position=37047639
|Orientation=plus
|GMAF=0.004132
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=G,T
|CAF=0.9959; 0.004132; .
|CHROM=3
|CLNACC=RCV000075380.1; RCV000075381.1
|CLNALLE=1; 2
|CLNDBN=Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
|CLNHGVS=NC_000003.11:g.37089130A>G; NC_000003.11:g.37089130A>T
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=InSiGHT
|CLNSRCID=c.1852A>G; c.1852A>T
|COMMON=1
|Disease=Lynch syndrome
|FwdALT=G,T
|FwdREF=A
|GENEINFO=MLH1:4292
|GENE_ID=4292
|GENE_NAME=MLH1
|REF=A
|RSPOS=37089130
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050268000000040516100100
|WGT=0
|dbSNPBuildID=126
|rsid=35001569
}}

{{on chip | FTDNA}}