{{Rsnum
|rsid=137852867
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HPD
|position=121847211
|Gene_s=HPD
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=609695
|variant=0003
|rsnum=137852867
}}{{ClinVar
|rsid=137852867
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=122285117
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HPD:3242
|GENE_NAME=HPD
|GENE_ID=3242
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.122285117G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609695.0003
|CLNSIG=5
|CLNCUI=C0268623
|CLNDBN=4-Hydroxyphenylpyruvate dioxygenase deficiency
|Disease=4-Hydroxyphenylpyruvate dioxygenase deficiency
|CLNACC=RCV000001641.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268623:276710:69723:413356003
}}