Have questions? Visit https://www.reddit.com/r/SNPedia

rs199475584

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199475584(A;T)
Make rs199475584(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position102843648
GenePAH
is asnp
is mentioned by
dbSNPrs199475584
ebirs199475584
HLIrs199475584
Exacrs199475584
Varsomers199475584
Maprs199475584
PheGenIrs199475584
hapmaprs199475584
1000 genomesrs199475584
hgdprs199475584
ensemblrs199475584
gopubmedrs199475584
geneviewrs199475584
scholarrs199475584
googlers199475584
pharmgkbrs199475584
gwascentralrs199475584
openSNPrs199475584
23andMers199475584
23andMe allrs199475584
SNP Nexus

SNPshotrs199475584
SNPdbers199475584
MSV3drs199475584
GWAS Ctlgrs199475584
Max Magnitude0
ClinVar
Risk rs199475584(T;T)
Alt rs199475584(T;T)
Reference rs199475584(A;A)
Significance Pathogenic
Disease Phenylketonuria not provided
Variation info
Gene PAH
CLNDBN Phenylketonuria not provided
Reversed 1
HGVS NC_000012.11:g.103237426T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000632.3, RCV000088786.1,