{{Rsnum
|rsid=5030856
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PAH
|position=102843676
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=5030856
|variant=0051
}}

{{ClinVar
|rsid=5030856
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=103237454
|CHROM=12
|dbSNPBuildID=113
|SSR=0
|SAO=1
|VP=0x050360000000000402110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.103237454T>C
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=3987; 612349.0051
|CLNSIG=5
|CLNCUI=C0751435; C0031485
|CLNDBN=Hyperphenylalaninemia, non-pku; Phenylketonuria; not provided
|Disease=Hyperphenylalaninemia; Phenylketonuria; not provided
|CLNACC=RCV000000656.2; RCV000000657.2; RCV000078503.1
|Tags=RV;PM;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C0751435; NBK1504:C0031485:261600:2209:716:154735006
}}

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