rs17075286

Orientation

plus

Stabilized

plus

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

Make rs17075286(C;G)

Make rs17075286(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

43189231

is a	snp
is	mentioned by
dbSNP	rs17075286
dbSNP (classic)	rs17075286
ClinGen	rs17075286
ebi	rs17075286
HLI	rs17075286
Exac	rs17075286
Gnomad	rs17075286
Varsome	rs17075286
LitVar	rs17075286
Map	rs17075286
PheGenI	rs17075286
Biobank	rs17075286
1000 genomes	rs17075286
hgdp	rs17075286
ensembl	rs17075286
geneview	rs17075286
scholar	rs17075286
google	rs17075286
pharmgkb	rs17075286
gwascentral	rs17075286
openSNP	rs17075286
23andMe	rs17075286
SNPshot	rs17075286
SNPdbe	rs17075286
MSV3d	rs17075286
GWAS Ctlg	rs17075286

GMAF

0.07759

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21057379]
Trait
Title	Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
Risk Allele
P-val	8E-7
Odds Ratio	None None