{{Rsnum
|rsid=121912958
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MLH1
|position=37012098
|Gene_s=MLH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=63751615
}}{{omim
|id=120436
|variant=0010
|rsnum=121912958
}}{{ClinVar
|rsid=121912958
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37053589
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=050260400611000002110100
|GENEINFO=MLH1:4292
|GENE_NAME=MLH1
|GENE_ID=4292
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.37053589C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120436.0010; 120436.0010
|CLNSIG=5
|CLNCUI=C1333991; C0265325
|CLNDBN=Lynch syndrome II; Turcot syndrome
|Disease=Lynch syndrome II; Turcot syndrome
|CLNACC=SCV000038899.1; SCV000038900.1
|Tags=PM;S3D;NSN;REF;U5;OTH;OTHERKG;LSD;OM
}}