rs4027132

plus

Geno	Mag	Summary
(A;A)	2	1.51x increased risk of developing bipolar disorder
(A;G)	1.5	1.39x increased risk of developing bipolar disorder
(G;G)	1	Normal risk of developing bipolar disorder

Reference

GRCh38 38.1/141

Chromosome

2

Position

11897366

is a	snp
is	mentioned by
dbSNP	rs4027132
dbSNP (classic)	rs4027132
ClinGen	rs4027132
ebi	rs4027132
HLI	rs4027132
Exac	rs4027132
Gnomad	rs4027132
Varsome	rs4027132
LitVar	rs4027132
Map	rs4027132
PheGenI	rs4027132
Biobank	rs4027132
1000 genomes	rs4027132
hgdp	rs4027132
ensembl	rs4027132
geneview	rs4027132
scholar	rs4027132
google	rs4027132
pharmgkb	rs4027132
gwascentral	rs4027132
openSNP	rs4027132
23andMe	rs4027132
SNPshot	rs4027132
SNPdbe	rs4027132
MSV3d	rs4027132
GWAS Ctlg	rs4027132

GMAF

0.4702

Max Magnitude

2

?

(A;A) (A;G) (G;G)

28

rs4027132 has been reported in a large study to be associated with bipolar disorder.

The risk allele (oriented to the dbSNP entry) is (A), and the odds ratio associated with heterozygotes is 1.39 (CI 1.19-1.64), and for homozygotes, 1.51 (CI 1.27-1.79). [PMID 17554300 ]

GWAS snp
PMID	[PMID 21254220 ]
Trait
Title	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val	0.000003
Odds Ratio	None None

[PMID 19567891 ] Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept.