rs7043482
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7043482(A;A) |
| Make rs7043482(A;C) |
| Make rs7043482(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 82521000 |
| Gene | LOC107987087 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7043482 |
| dbSNP (classic) | rs7043482 |
| ClinGen | rs7043482 |
| ebi | rs7043482 |
| HLI | rs7043482 |
| Exac | rs7043482 |
| Gnomad | rs7043482 |
| Varsome | rs7043482 |
| LitVar | rs7043482 |
| Map | rs7043482 |
| PheGenI | rs7043482 |
| Biobank | rs7043482 |
| 1000 genomes | rs7043482 |
| hgdp | rs7043482 |
| ensembl | rs7043482 |
| geneview | rs7043482 |
| scholar | rs7043482 |
| rs7043482 | |
| pharmgkb | rs7043482 |
| gwascentral | rs7043482 |
| openSNP | rs7043482 |
| 23andMe | rs7043482 |
| SNPshot | rs7043482 |
| SNPdbe | rs7043482 |
| MSV3d | rs7043482 |
| GWAS Ctlg | rs7043482 |
| GMAF | 0.4573 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | G |
| P-val | 0.000003 |
| Odds Ratio | 12.0000 [7.00 - 18.00] % increase |
[PMID 17434096] A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.
