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rs5941436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs5941436(A;A)
Make rs5941436(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position90033228
is asnp
is mentioned by
dbSNPrs5941436
ebirs5941436
HLIrs5941436
Exacrs5941436
Varsomers5941436
Maprs5941436
PheGenIrs5941436
hapmaprs5941436
1000 genomesrs5941436
hgdprs5941436
ensemblrs5941436
gopubmedrs5941436
geneviewrs5941436
scholarrs5941436
googlers5941436
pharmgkbrs5941436
gwascentralrs5941436
openSNPrs5941436
23andMers5941436
23andMe allrs5941436
SNP Nexus

SNPshotrs5941436
SNPdbers5941436
MSV3drs5941436
GWAS Ctlgrs5941436
GMAF0.1838
Max Magnitude0
? (A;A) (A;C) (C;C) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 5 x 10^-6) for Trails B performance
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000005
Odds Ratio None None