{{Rsnum
|rsid=398122386
|Chromosome=19
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CTC)
|geno3=(CTC;CTC)
|Gene=POLD1
|position=50408821
|Gene_s=POLD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000054542.24
|CLNALLE=1
|CLNDBN=Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN179768:615381:363649
|CLNHGVS=NC_000019.9:g.50912078_50912080delCTC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=174761.0003
|Disease=Mandibular hypoplasia
|FwdREF=CTC
|GENEINFO=POLD1:5424
|GENE_ID=5424
|GENE_NAME=POLD1
|REF=TCTC
|RSPOS=50912074
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398122386
}}