{{Rsnum
|rsid=62516095
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PAH
|position=102843777
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=62516095
|variant=0019
}}{{ClinVar
|rsid=62516095
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=103237555
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000000000402110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000012.11:g.103237555G>C; NC_000012.11:g.103237555G>T
|CLNORIGIN=1
|CLNSRCID=
612349.0019; 15883
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000000626.1; RCV000078501.1
|Tags=RV;PM;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDBN=Phenylketonuria; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1504:C0031485:261600:2209:716:154735006
|CLNSRC=OMIM Allelic Variant; Emory University
|Disease=Phenylketonuria; not provided
}}