{{Rsnum
|rsid=62516101
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PAH
|position=102843683
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=62516101
|variant=0045
}}{{ClinVar
|rsid=62516101
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=103237461
|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.103237461C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612349.0045
|CLNSIG=5
|CLNCUI=C0031485
|CLNDBN=Phenylketonuria
|Disease=Phenylketonuria
|CLNACC=RCV000000650.2
|Tags=RV;PM;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1504:C0031485:261600:2209:716:154735006
}}