rs6563353
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6563353(C;C) |
Make rs6563353(C;T) |
Make rs6563353(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 83556097 |
is a | snp |
is | mentioned by |
dbSNP | rs6563353 |
dbSNP (classic) | rs6563353 |
ClinGen | rs6563353 |
ebi | rs6563353 |
HLI | rs6563353 |
Exac | rs6563353 |
Gnomad | rs6563353 |
Varsome | rs6563353 |
LitVar | rs6563353 |
Map | rs6563353 |
PheGenI | rs6563353 |
Biobank | rs6563353 |
1000 genomes | rs6563353 |
hgdp | rs6563353 |
ensembl | rs6563353 |
geneview | rs6563353 |
scholar | rs6563353 |
rs6563353 | |
pharmgkb | rs6563353 |
gwascentral | rs6563353 |
openSNP | rs6563353 |
23andMe | rs6563353 |
SNPshot | rs6563353 |
SNPdbe | rs6563353 |
MSV3d | rs6563353 |
GWAS Ctlg | rs6563353 |
GMAF | 0.1511 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22760553![]() |
Trait | Response to citalopram treatment |
Title | Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D. |
Risk Allele | A |
P-val | 2E-6 |
Odds Ratio | NR NR |