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rs12559632

From SNPedia

Orientationplus
Stabilizedplus
Make rs12559632(A;A)
Make rs12559632(A;G)
Make rs12559632(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position22142875
GenePHEX
is asnp
is mentioned by
dbSNPrs12559632
ebirs12559632
HLIrs12559632
Exacrs12559632
Varsomers12559632
Maprs12559632
PheGenIrs12559632
hapmaprs12559632
1000 genomesrs12559632
hgdprs12559632
ensemblrs12559632
gopubmedrs12559632
geneviewrs12559632
scholarrs12559632
googlers12559632
pharmgkbrs12559632
gwascentralrs12559632
openSNPrs12559632
23andMers12559632
23andMe allrs12559632
SNP Nexus

SNPshotrs12559632
SNPdbers12559632
MSV3drs12559632
GWAS Ctlgrs12559632
GMAF0.3089
Max Magnitude
? (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