{{Rsnum
|rsid=104894453
|Chromosome=14
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PNP
|position=20474555
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PNP
}}{{omim
|id=164050
|rsnum=104894453
|variant=0001
}}{{ClinVar
|rsid=104894453
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=20942714
|CHROM=14
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PNP:4860
|GENE_NAME=PNP
|GENE_ID=4860
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000014.8:g.20942714G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164050.0001
|CLNSIG=5
|CLNCUI=C0268125
|CLNDBN=Purine-nucleoside phosphorylase deficiency
|Disease=Purine-nucleoside phosphorylase deficiency
|CLNACC=RCV000015025.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268125:613179:760:60743005
}}