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rs4397449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4397449(A;A)
Make rs4397449(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position89329957
is asnp
is mentioned by
dbSNPrs4397449
ebirs4397449
HLIrs4397449
Exacrs4397449
Varsomers4397449
Maprs4397449
PheGenIrs4397449
hapmaprs4397449
1000 genomesrs4397449
hgdprs4397449
ensemblrs4397449
gopubmedrs4397449
geneviewrs4397449
scholarrs4397449
googlers4397449
pharmgkbrs4397449
gwascentralrs4397449
openSNPrs4397449
23andMers4397449
23andMe allrs4397449
SNP Nexus

SNPshotrs4397449
SNPdbers4397449
MSV3drs4397449
GWAS Ctlgrs4397449
GMAF0.0202
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20125193OA-icon.png] non sig. gwas, hit (p = 3 x 10^-6) - Animals
GWAS snp
PMID [PMID 20125193OA-icon.png]
Trait Cognitive Performance
Title Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val 0.000003
Odds Ratio None None