{{Rsnum
|rsid=121434481
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HPGD
|position=174493236
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HPGD
}}{{omim
|id=601688
|rsnum=121434481
|variant=0004
}}{{ClinVar
|rsid=121434481
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=175414387
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HPGD:3248
|GENE_NAME=HPGD
|GENE_ID=3248
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.175414387A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601688.0004
|CLNSIG=5
|CLNCUI=C1861514
|CLNDBN=Digital clubbing, isolated congenital
|Disease=Digital clubbing
|CLNACC=RCV000008382.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1861514:119900:217059
}}