rs969962

Orientation

plus

Stabilized

plus

Make rs969962(C;C)

Make rs969962(C;T)

Make rs969962(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

88110091

is a	snp
is	mentioned by
dbSNP	rs969962
dbSNP (classic)	rs969962
ClinGen	rs969962
ebi	rs969962
HLI	rs969962
Exac	rs969962
Gnomad	rs969962
Varsome	rs969962
LitVar	rs969962
Map	rs969962
PheGenI	rs969962
Biobank	rs969962
1000 genomes	rs969962
hgdp	rs969962
ensembl	rs969962
geneview	rs969962
scholar	rs969962
google	rs969962
pharmgkb	rs969962
gwascentral	rs969962
openSNP	rs969962
23andMe	rs969962
SNPshot	rs969962
SNPdbe	rs969962
MSV3d	rs969962
GWAS Ctlg	rs969962

GMAF

0.1529

Max Magnitude

0

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

GWAS snp
PMID	[PMID 19734545]
Trait	Cognitive performance
Title	A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Risk Allele
P-val	9E-6
Odds Ratio	NR NR