{{Rsnum
|rsid=104894455
|Chromosome=14
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PNP
|position=20472366
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PNP
}}{{omim
|id=164050
|rsnum=104894455
|variant=0008
}}{{ClinVar
|rsid=104894455
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=20940525
|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.20940525C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=164050.0008
|CLNSIG=5
|CLNCUI=C0268125
|CLNDBN=Purine-nucleoside phosphorylase deficiency
|Disease=Purine-nucleoside phosphorylase deficiency
|CLNACC=RCV000015032.20
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268125:613179:760:60743005
}}