rs16965962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common genotype |
| Make rs16965962(A;A) |
| Make rs16965962(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 105154672 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16965962 |
| dbSNP (classic) | rs16965962 |
| ClinGen | rs16965962 |
| ebi | rs16965962 |
| HLI | rs16965962 |
| Exac | rs16965962 |
| Gnomad | rs16965962 |
| Varsome | rs16965962 |
| LitVar | rs16965962 |
| Map | rs16965962 |
| PheGenI | rs16965962 |
| Biobank | rs16965962 |
| 1000 genomes | rs16965962 |
| hgdp | rs16965962 |
| ensembl | rs16965962 |
| geneview | rs16965962 |
| scholar | rs16965962 |
| rs16965962 | |
| pharmgkb | rs16965962 |
| gwascentral | rs16965962 |
| openSNP | rs16965962 |
| 23andMe | rs16965962 |
| SNPshot | rs16965962 |
| SNPdbe | rs16965962 |
| MSV3d | rs16965962 |
| GWAS Ctlg | rs16965962 |
| GMAF | 0.04729 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | T |
| P-val | 3E-7 |
| Odds Ratio | NR NR |
