rs9792548
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9792548(A;A) |
| Make rs9792548(A;G) |
| Make rs9792548(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 86958168 |
| Gene | GAS1RR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9792548 |
| dbSNP (classic) | rs9792548 |
| ClinGen | rs9792548 |
| ebi | rs9792548 |
| HLI | rs9792548 |
| Exac | rs9792548 |
| Gnomad | rs9792548 |
| Varsome | rs9792548 |
| LitVar | rs9792548 |
| Map | rs9792548 |
| PheGenI | rs9792548 |
| Biobank | rs9792548 |
| 1000 genomes | rs9792548 |
| hgdp | rs9792548 |
| ensembl | rs9792548 |
| geneview | rs9792548 |
| scholar | rs9792548 |
| rs9792548 | |
| pharmgkb | rs9792548 |
| gwascentral | rs9792548 |
| openSNP | rs9792548 |
| 23andMe | rs9792548 |
| SNPshot | rs9792548 |
| SNPdbe | rs9792548 |
| MSV3d | rs9792548 |
| GWAS Ctlg | rs9792548 |
| GMAF | 0.4564 |
| 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 | 12.0000 [7.00 - 16.00] % decrease |
