{{Rsnum
|rsid=137852868
|Gene=HPD
|Chromosome=12
|position=121839998
|Orientation=plus
|GMAF=0.0009183
|Gene_s=HPD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{omim
|id=609695
|variant=0004
|rsnum=137852868
}}{{ClinVar
|rsid=137852868
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=122277904
|CHROM=12
|GMAF=0.0009
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000016110100
|GENEINFO=HPD:3242
|GENE_NAME=HPD
|GENE_ID=3242
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.122277904G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609695.0004
|CLNSIG=5
|CLNCUI=C0268623
|CLNDBN=4-Hydroxyphenylpyruvate dioxygenase deficiency
|Disease=4-Hydroxyphenylpyruvate dioxygenase deficiency
|CLNACC=RCV000001642.2
|Tags=RV;PM;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268623:276710:69723:413356003
|COMMON=0
}}