{{Rsnum
|rsid=104894506
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=APRT
|position=88810550
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APRT
}}{{omim
|id=102600
|rsnum=104894506
|variant=0004
}}{{ClinVar
|rsid=104894506
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=88876958
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=APRT:353
|GENE_NAME=APRT
|GENE_ID=353
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.88876958T>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000030946.26; RCV000033903.2
|CLNDBN=Aprt deficiency; Deficiency of AMP pyrophorylase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK100238:C0268120:614723:976:124274002
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK100238; 102600.0004
|Disease=Aprt deficiency; Deficiency of AMP pyrophorylase
}}