{{Rsnum
|rsid=5030858
|Gene=PAH
|Chromosome=12
|position=102840493
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=5030858
|variant=0002
}}

{{ClinVar
|rsid=5030858
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=103234271
|CHROM=12
|GMAF=0.0009
|dbSNPBuildID=113
|SSR=0
|SAO=1
|VP=0x050360000000040516110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.103234271G>A
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1696; 612349.0002
|CLNSIG=5
|CLNCUI=C0031485
|CLNDBN=Phenylketonuria; not provided
|Disease=Phenylketonuria; not provided
|CLNACC=RCV000000607.2; RCV000078507.1
|Tags=RV;PM;S3D;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1504:C0031485:261600:2209:716:154735006
|COMMON=0
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}