rs17589516
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17589516(A;A) |
| Make rs17589516(A;G) |
| Make rs17589516(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 38068644 |
| Gene | ZFAND3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17589516 |
| dbSNP (classic) | rs17589516 |
| ClinGen | rs17589516 |
| ebi | rs17589516 |
| HLI | rs17589516 |
| Exac | rs17589516 |
| Gnomad | rs17589516 |
| Varsome | rs17589516 |
| LitVar | rs17589516 |
| Map | rs17589516 |
| PheGenI | rs17589516 |
| Biobank | rs17589516 |
| 1000 genomes | rs17589516 |
| hgdp | rs17589516 |
| ensembl | rs17589516 |
| geneview | rs17589516 |
| scholar | rs17589516 |
| rs17589516 | |
| pharmgkb | rs17589516 |
| gwascentral | rs17589516 |
| openSNP | rs17589516 |
| 23andMe | rs17589516 |
| SNPshot | rs17589516 |
| SNPdbe | rs17589516 |
| MSV3d | rs17589516 |
| GWAS Ctlg | rs17589516 |
| GMAF | 0.03581 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21901158 ]
|
| Trait | |
| Title | Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study. |
| Risk Allele | C |
| P-val | 0.000004 |
| Odds Ratio | 45.0000 [24.00 - 69.00] % increase |
