rs11827962

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0

Make rs11827962(C;T)

Make rs11827962(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

22291020

is a	snp
is	mentioned by
dbSNP	rs11827962
dbSNP (classic)	rs11827962
ClinGen	rs11827962
ebi	rs11827962
HLI	rs11827962
Exac	rs11827962
Gnomad	rs11827962
Varsome	rs11827962
LitVar	rs11827962
Map	rs11827962
PheGenI	rs11827962
Biobank	rs11827962
1000 genomes	rs11827962
hgdp	rs11827962
ensembl	rs11827962
geneview	rs11827962
scholar	rs11827962
google	rs11827962
pharmgkb	rs11827962
gwascentral	rs11827962
openSNP	rs11827962
23andMe	rs11827962
SNPshot	rs11827962
SNPdbe	rs11827962
MSV3d	rs11827962
GWAS Ctlg	rs11827962

GMAF

0.01561

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23453885]
Trait	Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title	Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele	C
P-val	6E-6
Odds Ratio	1.04 [0.94-1.15]