{{Rsnum
|rsid=104894507
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=APRT
|position=88810450
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APRT
}}{{omim
|id=102600
|rsnum=104894507
|variant=0005
}}{{ClinVar
|rsid=104894507
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=88876858
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=APRT:353
|GENE_NAME=APRT
|GENE_ID=353
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.88876858C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000030947.26; RCV000033905.2
|CLNDBN=Aprt deficiency; Deficiency of AMP pyrophorylase
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=102600.0005
|Disease=Aprt deficiency; Deficiency of AMP pyrophorylase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK100238:C0268120:614723:976:124274002
}}