rs11648716
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11648716(A;A) |
| Make rs11648716(A;G) |
| Make rs11648716(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 85873010 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11648716 |
| dbSNP (classic) | rs11648716 |
| ClinGen | rs11648716 |
| ebi | rs11648716 |
| HLI | rs11648716 |
| Exac | rs11648716 |
| Gnomad | rs11648716 |
| Varsome | rs11648716 |
| LitVar | rs11648716 |
| Map | rs11648716 |
| PheGenI | rs11648716 |
| Biobank | rs11648716 |
| 1000 genomes | rs11648716 |
| hgdp | rs11648716 |
| ensembl | rs11648716 |
| geneview | rs11648716 |
| scholar | rs11648716 |
| rs11648716 | |
| pharmgkb | rs11648716 |
| gwascentral | rs11648716 |
| openSNP | rs11648716 |
| 23andMe | rs11648716 |
| SNPshot | rs11648716 |
| SNPdbe | rs11648716 |
| MSV3d | rs11648716 |
| GWAS Ctlg | rs11648716 |
| GMAF | 0.04683 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | G |
| P-val | 7E-6 |
| Odds Ratio | 39.68 [22.37-56.99] mg/dL decrease |
