{{Rsnum
|rsid=387906725
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HPRT1
|position=134475189
|Gene_s=HPRT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000022877.2; RCV000022878.2
|CLNALLE=1
|CLNDBN=Lesch-nyhan syndrome, neurologic variant; Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1845893; C0268117:300323:79233:238007004
|CLNHGVS=NC_000023.10:g.133609219G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=308000.0060
|Disease=Lesch-nyhan syndrome; Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=133609219
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906725
|GENEINFO=HPRT1:3251
|GENE_ID=3251
|GENE_NAME=HPRT1
}}