{{Rsnum
|rsid=137852481
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HPRT1
|position=134475268
|Gene_s=HPRT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308000
|variant=0008
|rsnum=137852481
}}{{ClinVar
|rsid=137852481
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=133609298
|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.133609298C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=308000.0008
|CLNSIG=255
|CLNCUI=C0023374
|CLNDBN=Lesch-Nyhan syndrome; HPRT FLINT
|Disease=Lesch-Nyhan syndrome; HPRT FLINT
|CLNACC=RCV000010726.1; RCV000010727.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1149:C0023374:300322:510:10406007
}}