rs4650608

Orientation

plus

Stabilized

plus

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

Make rs4650608(C;C)

Make rs4650608(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

78772330

is a	snp
is	mentioned by
dbSNP	rs4650608
dbSNP (classic)	rs4650608
ClinGen	rs4650608
ebi	rs4650608
HLI	rs4650608
Exac	rs4650608
Gnomad	rs4650608
Varsome	rs4650608
LitVar	rs4650608
Map	rs4650608
PheGenI	rs4650608
Biobank	rs4650608
1000 genomes	rs4650608
hgdp	rs4650608
ensembl	rs4650608
geneview	rs4650608
scholar	rs4650608
google	rs4650608
pharmgkb	rs4650608
gwascentral	rs4650608
openSNP	rs4650608
23andMe	rs4650608
SNPshot	rs4650608
SNPdbe	rs4650608
MSV3d	rs4650608
GWAS Ctlg	rs4650608

GMAF

0.2291

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22182935]
Trait
Title	Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
Risk Allele	T
P-val	0.000001
Odds Ratio	None None

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	1E-6
Odds Ratio	1.06 [1.03-1.09]

GWAS snp
PMID	[PMID 24280982]
Trait	Schizophrenia or bipolar disorder
Title	Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
Risk Allele
P-val	8E-9
Odds Ratio	NR NR