{{Rsnum
|rsid=104894274
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTS
|position=112226489
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTS
}}{{omim
|id=612719
|rsnum=104894274
|variant=0002
}}{{ClinVar
|rsid=104894274
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=112097212
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PTS:5805
|GENE_NAME=PTS
|GENE_ID=5805
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.112097212C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612719.0002
|CLNSIG=5
|CLNCUI=CN068421
|CLNDBN=Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency
|Disease=Hyperphenylalaninemia
|CLNACC=RCV000000506.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN068421
}}