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rs492478

From SNPedia

Orientationplus
Stabilizedplus
Make rs492478(A;A)
Make rs492478(A;G)
Make rs492478(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position3939362
is asnp
is mentioned by
dbSNPrs492478
ebirs492478
HLIrs492478
Exacrs492478
Varsomers492478
Maprs492478
PheGenIrs492478
hapmaprs492478
1000 genomesrs492478
hgdprs492478
ensemblrs492478
gopubmedrs492478
geneviewrs492478
scholarrs492478
googlers492478
pharmgkbrs492478
gwascentralrs492478
openSNPrs492478
23andMers492478
23andMe allrs492478
SNP Nexus

SNPshotrs492478
SNPdbers492478
MSV3drs492478
GWAS Ctlgrs492478
GMAF0.1983
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 4 x 10^-6) for Stroop test 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 0.000004
Odds Ratio None None