rs7662358

Orientation

plus

Stabilized

plus

Make rs7662358(A;A)

Make rs7662358(A;C)

Make rs7662358(C;C)

Reference

GRCh38 38.1/141

Chromosome

4

Position

188669705

is a	snp
is	mentioned by
dbSNP	rs7662358
dbSNP (classic)	rs7662358
ClinGen	rs7662358
ebi	rs7662358
HLI	rs7662358
Exac	rs7662358
Gnomad	rs7662358
Varsome	rs7662358
LitVar	rs7662358
Map	rs7662358
PheGenI	rs7662358
Biobank	rs7662358
1000 genomes	rs7662358
hgdp	rs7662358
ensembl	rs7662358
geneview	rs7662358
scholar	rs7662358
google	rs7662358
pharmgkb	rs7662358
gwascentral	rs7662358
openSNP	rs7662358
23andMe	rs7662358
SNPshot	rs7662358
SNPdbe	rs7662358
MSV3d	rs7662358
GWAS Ctlg	rs7662358

GMAF

0.1373

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

GWAS snp
PMID	[PMID 20125193]
Trait	Cognitive performance
Title	Common genetic variation and performance on standardized cognitive tests.
Risk Allele
P-val	9E-6
Odds Ratio	NR NR