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rs1522305

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) normal
(C;G) normal
(G;G) slightly increased risk for schizophrenia
ReferenceGRCh38 38.1/141
Chromosome12
Position102886978
GenePAH
is asnp
is mentioned by
dbSNPrs1522305
ebirs1522305
HLIrs1522305
Exacrs1522305
Varsomers1522305
Maprs1522305
PheGenIrs1522305
hapmaprs1522305
1000 genomesrs1522305
hgdprs1522305
ensemblrs1522305
gopubmedrs1522305
geneviewrs1522305
scholarrs1522305
googlers1522305
pharmgkbrs1522305
gwascentralrs1522305
openSNPrs1522305
23andMers1522305
23andMe allrs1522305
SNP Nexus

SNPshotrs1522305
SNPdbers1522305
MSV3drs1522305
GWAS Ctlgrs1522305
GMAF0.1644
Max Magnitude
? (C;C) (C;G) (G;G) 28
rs1522305 is a SNP in the phenylalanine hydroxylase (PAH) gene.

A study of Caucasian cohorts, Bulgarian families, and African American families concluded that the more common rs1522305(G) allele was associated in the first two populations with increased risk for schizophrenia. [PMID 18937293OA-icon.png]