{{Rsnum
|rsid=121434480
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HPGD
|position=174508699
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HPGD
}}{{omim
|id=601688
|rsnum=121434480
|variant=0001
}}{{ClinVar
|rsid=121434480
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=175429850
|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.175429850C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000008379.3
|CLNDBN=Cranioosteoarthropathy
|CLNDSDB=MedGen
|CLNDSDBID=C2678439
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601688.0001
|Disease=Cranioosteoarthropathy
}}