{{Rsnum
|rsid=137852495
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HPRT1
|position=134475216
|Gene_s=HPRT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=308000
|variant=0036
|rsnum=137852495
}}{{ClinVar
|rsid=137852495
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=133609246
|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.133609246T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=308000.0036
|CLNSIG=255
|CLNCUI=C1845893
|CLNDBN=Lesch-nyhan syndrome, neurologic variant; HPRT MONTREAL
|Disease=Lesch-nyhan syndrome; HPRT MONTREAL
|CLNACC=RCV000010763.1; RCV000010764.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1845893
}}