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rs11055387

From SNPedia

Orientationplus
Stabilizedplus
Make rs11055387(C;C)
Make rs11055387(C;G)
Make rs11055387(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position13367062
is asnp
is mentioned by
dbSNPrs11055387
dbSNP (classic)rs11055387
ClinGenrs11055387
ebirs11055387
HLIrs11055387
Exacrs11055387
Gnomadrs11055387
Varsomers11055387
LitVarrs11055387
Maprs11055387
PheGenIrs11055387
Biobankrs11055387
1000 genomesrs11055387
hgdprs11055387
ensemblrs11055387
geneviewrs11055387
scholarrs11055387
googlers11055387
pharmgkbrs11055387
gwascentralrs11055387
openSNPrs11055387
23andMers11055387
SNPshotrs11055387
SNPdbers11055387
MSV3drs11055387
GWAS Ctlgrs11055387
GMAF0.09045
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 23377640OA-icon.png]
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 8E-6
Odds Ratio 2.19 [1.84-2.53]