{{Rsnum
|rsid=104894508
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=APRT
|position=88810141
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APRT
}}{{omim
|id=102600
|rsnum=104894508
|variant=0007
}}{{ClinVar
|rsid=104894508
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=88876549
|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.88876549A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019962.25
|CLNDBN=Aprt deficiency
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=102600.0007
|Disease=Aprt deficiency
}}