{{Rsnum
|rsid=62508646
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PAH
|position=102844356
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=62508646
|variant=0041
}}

{{ClinVar
|rsid=62508646
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=103238134
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000000000402110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000012.11:g.103238134A>G
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1708; 612349.0041
|CLNSIG=5
|CLNCUI=C0031485
|CLNDBN=Phenylketonuria; not provided
|Disease=Phenylketonuria; not provided
|CLNACC=RCV000000646.1; RCV000078499.1
|Tags=RV;PM;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1504:C0031485:261600:2209:716:154735006
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}