rs10508921
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10508921(C;C) |
| Make rs10508921(C;T) |
| Make rs10508921(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 50250948 |
| Gene | ASAH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10508921 |
| dbSNP (classic) | rs10508921 |
| ClinGen | rs10508921 |
| ebi | rs10508921 |
| HLI | rs10508921 |
| Exac | rs10508921 |
| Gnomad | rs10508921 |
| Varsome | rs10508921 |
| LitVar | rs10508921 |
| Map | rs10508921 |
| PheGenI | rs10508921 |
| Biobank | rs10508921 |
| 1000 genomes | rs10508921 |
| hgdp | rs10508921 |
| ensembl | rs10508921 |
| geneview | rs10508921 |
| scholar | rs10508921 |
| rs10508921 | |
| pharmgkb | rs10508921 |
| gwascentral | rs10508921 |
| openSNP | rs10508921 |
| 23andMe | rs10508921 |
| SNPshot | rs10508921 |
| SNPdbe | rs10508921 |
| MSV3d | rs10508921 |
| GWAS Ctlg | rs10508921 |
| GMAF | 0.1625 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | T |
| P-val | 9E-7 |
| Odds Ratio | 25.70 [15.47-35.93] mg/dL decrease |
