rs12559632
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12559632(A;A) |
Make rs12559632(A;G) |
Make rs12559632(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 22142875 |
Gene | PHEX |
is a | snp |
is | mentioned by |
dbSNP | rs12559632 |
dbSNP (classic) | rs12559632 |
ClinGen | rs12559632 |
ebi | rs12559632 |
HLI | rs12559632 |
Exac | rs12559632 |
Gnomad | rs12559632 |
Varsome | rs12559632 |
LitVar | rs12559632 |
Map | rs12559632 |
PheGenI | rs12559632 |
Biobank | rs12559632 |
1000 genomes | rs12559632 |
hgdp | rs12559632 |
ensembl | rs12559632 |
geneview | rs12559632 |
scholar | rs12559632 |
rs12559632 | |
pharmgkb | rs12559632 |
gwascentral | rs12559632 |
openSNP | rs12559632 |
23andMe | rs12559632 |
SNPshot | rs12559632 |
SNPdbe | rs12559632 |
MSV3d | rs12559632 |
GWAS Ctlg | rs12559632 |
GMAF | 0.3089 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21326311] |
Trait | |
Title | Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients |
Risk Allele | A |
P-val | 0.000003 |
Odds Ratio | 1.1600 [0.69-1.63] unit decrease |