{{Rsnum
|rsid=80338676
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRPS1
|position=107642415
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRPS1
}}{{omim
|id=311850
|rsnum=80338676
|variant=0011
}}{{ClinVar
|rsid=80338676
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=106885645
|CHROM=X
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=PRPS1:5631
|GENE_NAME=PRPS1
|GENE_ID=5631
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.106885645T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK2591; 311850.0011
|CLNSIG=5
|CLNCUI=C0796028; C0796028
|CLNDBN=Arts syndrome
|Disease=Arts syndrome
|CLNACC=RCV000010614.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1876:NBK2591:C0796028:301835:1187
}}{{PMID Auto
|PMID=17701896
|Title=Arts syndrome is caused by loss-of-function mutations in PRPS1.
|OA=1
}}