{{Rsnum
|rsid=137852487
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HPRT1
|position=134475255
|Gene_s=HPRT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308000
|variant=0016
|rsnum=137852487
}}{{ClinVar
|rsid=137852487
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=133609285
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HPRT1:3251
|GENE_NAME=HPRT1
|GENE_ID=3251
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.133609285G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=308000.0016
|CLNSIG=255
|CLNCUI=C0023374
|CLNDBN=Lesch-Nyhan syndrome; HPRT NEW HAVEN
|Disease=Lesch-Nyhan syndrome; HPRT NEW HAVEN
|CLNACC=RCV000010742.1; RCV000010743.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1149:C0023374:300322:510:10406007
}}