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rs199475668

From SNPedia

Orientationminus
Geno Mag Summary
(-;8) 3 Carrier of a phenylketonuria mutation
(GAACCGTG;GAACCGTG) 0 common in clinvar
Make rs199475668(-;-)
Make rs199475668(-;GAACCGTG)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102852812
GenePAH
is asnp
is mentioned by
dbSNPrs199475668
ebirs199475668
HLIrs199475668
Exacrs199475668
Varsomers199475668
Maprs199475668
PheGenIrs199475668
hapmaprs199475668
1000 genomesrs199475668
hgdprs199475668
ensemblrs199475668
gopubmedrs199475668
geneviewrs199475668
scholarrs199475668
googlers199475668
pharmgkbrs199475668
gwascentralrs199475668
openSNPrs199475668
23andMers199475668
23andMe allrs199475668
SNP Nexus

SNPshotrs199475668
SNPdbers199475668
MSV3drs199475668
GWAS Ctlgrs199475668
Max Magnitude3
ClinVar
Risk rs199475668(;)
Alt rs199475668(;)
Reference rs199475668(GAACCGTG;GAACCGTG)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103246590_103246597delCACGGTTC
CLNSRC
CLNACC RCV000089126.1,