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rs4625554

From SNPedia

Orientationplus
Stabilizedplus
Make rs4625554(A;A)
Make rs4625554(A;G)
Make rs4625554(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position4307138
GeneCCND2
is asnp
is mentioned by
dbSNPrs4625554
ebirs4625554
HLIrs4625554
Exacrs4625554
Varsomers4625554
Maprs4625554
PheGenIrs4625554
hapmaprs4625554
1000 genomesrs4625554
hgdprs4625554
ensemblrs4625554
gopubmedrs4625554
geneviewrs4625554
scholarrs4625554
googlers4625554
pharmgkbrs4625554
gwascentralrs4625554
openSNPrs4625554
23andMers4625554
23andMe allrs4625554
SNP Nexus

SNPshotrs4625554
SNPdbers4625554
MSV3drs4625554
GWAS Ctlgrs4625554
GMAF0.3113
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 9E-6
Odds Ratio .19 [0.11-0.28] unit increase


[PMID 18281541OA-icon.png] Effects of common germ-line genetic variation in cell cycle genes on ovarian cancer survival.


[PMID 18559547OA-icon.png] Comparing genetic ancestry and self-described race in african americans born in the United States and in Africa.