rs2099077
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2099077(G;G) |
| Make rs2099077(G;T) |
| Make rs2099077(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 103428347 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2099077 |
| dbSNP (classic) | rs2099077 |
| ClinGen | rs2099077 |
| ebi | rs2099077 |
| HLI | rs2099077 |
| Exac | rs2099077 |
| Gnomad | rs2099077 |
| Varsome | rs2099077 |
| LitVar | rs2099077 |
| Map | rs2099077 |
| PheGenI | rs2099077 |
| Biobank | rs2099077 |
| 1000 genomes | rs2099077 |
| hgdp | rs2099077 |
| ensembl | rs2099077 |
| geneview | rs2099077 |
| scholar | rs2099077 |
| rs2099077 | |
| pharmgkb | rs2099077 |
| gwascentral | rs2099077 |
| openSNP | rs2099077 |
| 23andMe | rs2099077 |
| SNPshot | rs2099077 |
| SNPdbe | rs2099077 |
| MSV3d | rs2099077 |
| GWAS Ctlg | rs2099077 |
| GMAF | 0.157 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23400010 ]
|
| Trait | Thiazide-induced adverse metabolic effects in hypertensive patients |
| Title | Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans. |
| Risk Allele | A |
| P-val | 8E-6 |
| Odds Ratio | 16.53 [9.26-23.8] mg/dL decrease |
