rs4397449

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs4397449(A;A)

Make rs4397449(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

89329957

is a	snp
is	mentioned by
dbSNP	rs4397449
dbSNP (classic)	rs4397449
ClinGen	rs4397449
ebi	rs4397449
HLI	rs4397449
Exac	rs4397449
Gnomad	rs4397449
Varsome	rs4397449
LitVar	rs4397449
Map	rs4397449
PheGenI	rs4397449
Biobank	rs4397449
1000 genomes	rs4397449
hgdp	rs4397449
ensembl	rs4397449
geneview	rs4397449
scholar	rs4397449
google	rs4397449
pharmgkb	rs4397449
gwascentral	rs4397449
openSNP	rs4397449
23andMe	rs4397449
SNPshot	rs4397449
SNPdbe	rs4397449
MSV3d	rs4397449
GWAS Ctlg	rs4397449

GMAF

0.0202

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 20125193] non sig. gwas, hit (p = 3 x 10^-6) - Animals

GWAS snp
PMID	[PMID 20125193]
Trait	Cognitive Performance
Title	Common genetic variation and performance on standardized cognitive tests
Risk Allele
P-val	0.000003
Odds Ratio	None None