rs11790994

Orientation

plus

Stabilized

plus

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

Make rs11790994(C;G)

Make rs11790994(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

95666984

is a	snp
is	mentioned by
dbSNP	rs11790994
dbSNP (classic)	rs11790994
ClinGen	rs11790994
ebi	rs11790994
HLI	rs11790994
Exac	rs11790994
Gnomad	rs11790994
Varsome	rs11790994
LitVar	rs11790994
Map	rs11790994
PheGenI	rs11790994
Biobank	rs11790994
1000 genomes	rs11790994
hgdp	rs11790994
ensembl	rs11790994
geneview	rs11790994
scholar	rs11790994
google	rs11790994
pharmgkb	rs11790994
gwascentral	rs11790994
openSNP	rs11790994
23andMe	rs11790994
SNPshot	rs11790994
SNPdbe	rs11790994
MSV3d	rs11790994
GWAS Ctlg	rs11790994

GMAF

0.1015

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

GWAS snp
PMID	[PMID 18821565]
Trait	Inattentive symptoms
Title	Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
Risk Allele
P-val	2E-7
Odds Ratio	NR NR