rs9601248

Orientation

plus

Stabilized

plus

Make rs9601248(C;C)

Make rs9601248(C;T)

Make rs9601248(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

79594869

is a	snp
is	mentioned by
dbSNP	rs9601248
dbSNP (classic)	rs9601248
ClinGen	rs9601248
ebi	rs9601248
HLI	rs9601248
Exac	rs9601248
Gnomad	rs9601248
Varsome	rs9601248
LitVar	rs9601248
Map	rs9601248
PheGenI	rs9601248
Biobank	rs9601248
1000 genomes	rs9601248
hgdp	rs9601248
ensembl	rs9601248
geneview	rs9601248
scholar	rs9601248
google	rs9601248
pharmgkb	rs9601248
gwascentral	rs9601248
openSNP	rs9601248
23andMe	rs9601248
SNPshot	rs9601248
SNPdbe	rs9601248
MSV3d	rs9601248
GWAS Ctlg	rs9601248

GMAF

0.4646

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23377640]
Trait	Major depressive disorder
Title	Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.
Risk Allele	C
P-val	2E-6
Odds Ratio	1.38 [1.25-1.52]