rs916829
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs916829(C;C) |
| Make rs916829(C;T) |
| Make rs916829(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 17418926 |
| Gene | ABCC8 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs916829 |
| dbSNP (classic) | rs916829 |
| ClinGen | rs916829 |
| ebi | rs916829 |
| HLI | rs916829 |
| Exac | rs916829 |
| Gnomad | rs916829 |
| Varsome | rs916829 |
| LitVar | rs916829 |
| Map | rs916829 |
| PheGenI | rs916829 |
| Biobank | rs916829 |
| 1000 genomes | rs916829 |
| hgdp | rs916829 |
| ensembl | rs916829 |
| geneview | rs916829 |
| scholar | rs916829 |
| rs916829 | |
| pharmgkb | rs916829 |
| gwascentral | rs916829 |
| openSNP | rs916829 |
| 23andMe | rs916829 |
| SNPshot | rs916829 |
| SNPdbe | rs916829 |
| MSV3d | rs916829 |
| GWAS Ctlg | rs916829 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25867398] Associations between genetic variants and the severity of metabolic syndrome in subjects with type 2 diabetes
