rs2506933

Orientation

plus

Stabilized

plus

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

Make rs2506933(C;C)

Make rs2506933(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

92905732

is a	snp
is	mentioned by
dbSNP	rs2506933
dbSNP (classic)	rs2506933
ClinGen	rs2506933
ebi	rs2506933
HLI	rs2506933
Exac	rs2506933
Gnomad	rs2506933
Varsome	rs2506933
LitVar	rs2506933
Map	rs2506933
PheGenI	rs2506933
Biobank	rs2506933
1000 genomes	rs2506933
hgdp	rs2506933
ensembl	rs2506933
geneview	rs2506933
scholar	rs2506933
google	rs2506933
pharmgkb	rs2506933
gwascentral	rs2506933
openSNP	rs2506933
23andMe	rs2506933
SNPshot	rs2506933
SNPdbe	rs2506933
MSV3d	rs2506933
GWAS Ctlg	rs2506933

GMAF

0.2388

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 20125193] non sig. gwas, hit (p = 6 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	0.000006
Odds Ratio	None None