{{Rsnum
|rsid=199473690
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=DNMT1
|position=10155017
|Gene_s=DNMT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199473690
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=10265693
|CHROM=19
|dbSNPBuildID=136
|SSR=0
|SAO=0
|VP=0x050360000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.10265693T>C
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=126375.0001
|CLNSIG=5
|CLNCUI=CN077692
|CLNDBN=NEUROPATHY, HEREDITARY SENSORY, TYPE IE
|Disease=NEUROPATHY
|CLNACC=RCV000022529.25
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1133:NBK84112:C3279885:614116
|GENEINFO=DNMT1:1786
|GENE_ID=1786
|GENE_NAME=DNMT1
}}