rs1522305
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | normal | |
(C;G) | normal | |
(G;G) | slightly increased risk for schizophrenia |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 102886978 |
Gene | PAH |
is a | snp |
is | mentioned by |
dbSNP | rs1522305 |
dbSNP (classic) | rs1522305 |
ClinGen | rs1522305 |
ebi | rs1522305 |
HLI | rs1522305 |
Exac | rs1522305 |
Gnomad | rs1522305 |
Varsome | rs1522305 |
LitVar | rs1522305 |
Map | rs1522305 |
PheGenI | rs1522305 |
Biobank | rs1522305 |
1000 genomes | rs1522305 |
hgdp | rs1522305 |
ensembl | rs1522305 |
geneview | rs1522305 |
scholar | rs1522305 |
rs1522305 | |
pharmgkb | rs1522305 |
gwascentral | rs1522305 |
openSNP | rs1522305 |
23andMe | rs1522305 |
SNPshot | rs1522305 |
SNPdbe | rs1522305 |
MSV3d | rs1522305 |
GWAS Ctlg | rs1522305 |
GMAF | 0.1644 |
Max Magnitude | 0 |
? | (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 18937293]