{{Rsnum
|rsid = 28999113
|Gene = APRT
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|Chromosome=16
|position=88809834
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=APRT
}}{{omim
|desc=APRT DEFICIENCY, JAPANESE TYPE
|id=102600
|rsnum=28999113
|variant=0003
}}

{{ClinVar
|rsid=28999113
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=88876242
|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.88876242A>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000019958.26; RCV000033908.2
|CLNDBN=APRT deficiency, Japanese type; Deficiency of AMP pyrophorylase
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268121; NBK100238:C0268120:614723:976:124274002
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK100238; 102600.0003
|Disease=APRT deficiency; Deficiency of AMP pyrophorylase
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}