rs591044
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs591044(C;C) |
| Make rs591044(C;T) |
| Make rs591044(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 26301229 |
| Gene | SEZ6L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs591044 |
| dbSNP (classic) | rs591044 |
| ClinGen | rs591044 |
| ebi | rs591044 |
| HLI | rs591044 |
| Exac | rs591044 |
| Gnomad | rs591044 |
| Varsome | rs591044 |
| LitVar | rs591044 |
| Map | rs591044 |
| PheGenI | rs591044 |
| Biobank | rs591044 |
| 1000 genomes | rs591044 |
| hgdp | rs591044 |
| ensembl | rs591044 |
| geneview | rs591044 |
| scholar | rs591044 |
| rs591044 | |
| pharmgkb | rs591044 |
| gwascentral | rs591044 |
| openSNP | rs591044 |
| 23andMe | rs591044 |
| SNPshot | rs591044 |
| SNPdbe | rs591044 |
| MSV3d | rs591044 |
| GWAS Ctlg | rs591044 |
| GMAF | 0.3848 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | A |
| P-val | 0.000006 |
| Odds Ratio | 9.0000 [5.00 - 13.00] % increase |
