rs6990255

Orientation

plus

Stabilized

plus

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

Make rs6990255(C;T)

Make rs6990255(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

34269430

is a	snp
is	mentioned by
dbSNP	rs6990255
dbSNP (classic)	rs6990255
ClinGen	rs6990255
ebi	rs6990255
HLI	rs6990255
Exac	rs6990255
Gnomad	rs6990255
Varsome	rs6990255
LitVar	rs6990255
Map	rs6990255
PheGenI	rs6990255
Biobank	rs6990255
1000 genomes	rs6990255
hgdp	rs6990255
ensembl	rs6990255
geneview	rs6990255
scholar	rs6990255
google	rs6990255
pharmgkb	rs6990255
gwascentral	rs6990255
openSNP	rs6990255
23andMe	rs6990255
SNPshot	rs6990255
SNPdbe	rs6990255
MSV3d	rs6990255
GWAS Ctlg	rs6990255

GMAF

0.09183

Max Magnitude

0

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

GWAS snp
PMID	[PMID 19416921]
Trait	Bipolar disorder
Title	Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry
Risk Allele	T
P-val	0.000006
Odds Ratio	1.33 [1.18-1.51]

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	T
P-val	2E-6
Odds Ratio	1.15 [1.09-1.20]