{{Rsnum
|rsid=75193786
|Gene=PAH
|Chromosome=12
|position=102894893
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PAH
}}{{omim
|id=612349
|rsnum=75193786
|variant=0063
}}{{ClinVar
|rsid=75193786
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=103288671
|CHROM=12
|GMAF=0.0005
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050360000000000416110104
|GENEINFO=PAH:5053
|GENE_NAME=PAH
|GENE_ID=5053
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000012.11:g.103288671A>G
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=1707; 612349.0063
|CLNSIG=5
|CLNCUI=C0031485
|CLNDBN=Phenylketonuria; not provided
|Disease=Phenylketonuria; not provided
|CLNACC=RCV000000668.1; RCV000078516.1
|Tags=RV;PM;S3D;SLO;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM;NOV
|CAF=0.9995; 0.0004591; .
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1504:C0031485:261600:2209:716:154735006
|COMMON=0
}}