{{Rsnum
|rsid=63750899
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MLH1
|position=37048562
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MLH1
}}{{omim
|id=120436
|rsnum=63750899
|variant=0020
}}

{{ClinVar
|rsid=63750899
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37090053
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MLH1:4292
|GENE_NAME=MLH1
|GENE_ID=4292
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.37090053C>T
|CLNSRC=InSiGHT; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=c.1942C>T; 120436.0020
|CLNSIG=5
|CLNCUI=C1333991; C0265325
|CLNDBN=Lynch syndrome II; Turcot syndrome; Lynch syndrome
|Disease=Lynch syndrome II; Turcot syndrome; Lynch syndrome
|CLNACC=RCV000018629.22; RCV000018630.26; RCV000075432.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C1333991:609310:144; NBK1211:C0265325:276300:252202:61665008; NBK1211:C0009405:315058005
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}