{{Rsnum
|rsid=35502531
|Chromosome=3
|Orientation=plus
|geno1=(AA;AA)
|geno2=(AA;GC)
|geno3=(GC;GC)
|Gene=MLH1
|position=37047639
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MLH1
}}{{omim
|id=120436
|rsnum=35502531
|variant=0012
}}{{ClinVar
|rsid=35502531
|Reversed=0
|FwdREF=AA
|FwdALT=GC
|REF=GAA
|ALT=GGC
|RSPOS=37089129
|CHROM=3
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050260000000000002110800
|GENEINFO=MLH1:4292
|GENE_NAME=MLH1
|GENE_ID=4292
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=
NC_000003.11:g.37089130_37089131delAAinsGC
|CLNORIGIN=1
|CLNSRCID=
c.1852_1853delinsGC; 120436.0012
|CLNSIG=2
|CLNCUI=
|CLNACC=
RCV000018620.1; RCV000034542.1; RCV000075382.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDBN=Reclassified - variant of unknown significance; not provided; Lynch syndrome
|CLNSRC=InSiGHT; OMIM Allelic Variant
|Disease=Reclassified - variant of unknown significance; not provided; Lynch syndrome
|CLNDSDB=GeneReviews:MedGen:SNOMED_CT
|CLNDSDBID=NBK1211:C0009405:315058005
}}