{{Rsnum
|rsid=118203925
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PAH
|position=102912819
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=118203925
|variant=0056
}}{{ClinVar
|rsid=118203925
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=103306597
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.103306597G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612349.0056
|CLNSIG=5
|CLNCUI=C0751435
|CLNDBN=Hyperphenylalaninemia, non-pku
|Disease=Hyperphenylalaninemia
|CLNACC=RCV000000662.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C0751435
}}