{{Rsnum
|rsid=5030860
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PAH
|position=102840474
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=5030860
|variant=0017
}}

{{ClinVar
|rsid=5030860
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=103234252
|CHROM=12
|dbSNPBuildID=113
|SSR=16
|SAO=1
|VP=0x05036000000004050e110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.103234252T>C
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1690; 612349.0017
|CLNSIG=5
|CLNCUI=C0751435
|CLNDBN=Hyperphenylalaninemia, non-pku; not provided
|Disease=Hyperphenylalaninemia; not provided
|CLNACC=RCV000000624.1; RCV000078508.1
|Tags=RV;PM;S3D;SLO;VLD;HD;GNO;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C0751435
}}

{{on chip | FTDNA2}}
{{on chip | FTDNA}}