rs1706631
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1706631(A;A) |
Make rs1706631(A;T) |
Make rs1706631(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 17509301 |
is a | snp |
is | mentioned by |
dbSNP | rs1706631 |
dbSNP (classic) | rs1706631 |
ClinGen | rs1706631 |
ebi | rs1706631 |
HLI | rs1706631 |
Exac | rs1706631 |
Gnomad | rs1706631 |
Varsome | rs1706631 |
LitVar | rs1706631 |
Map | rs1706631 |
PheGenI | rs1706631 |
Biobank | rs1706631 |
1000 genomes | rs1706631 |
hgdp | rs1706631 |
ensembl | rs1706631 |
geneview | rs1706631 |
scholar | rs1706631 |
rs1706631 | |
pharmgkb | rs1706631 |
gwascentral | rs1706631 |
openSNP | rs1706631 |
23andMe | rs1706631 |
SNPshot | rs1706631 |
SNPdbe | rs1706631 |
MSV3d | rs1706631 |
GWAS Ctlg | rs1706631 |
GMAF | 0.455 |
Max Magnitude | 0 |
? | (A;A) (A;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 | T |
P-val | 6E-6 |
Odds Ratio | 1.35 [1.22-1.49] |