| RSID | rs71040457 |
| HGVS | NC_000002.11:g.220294782_220294783insG |
| Chromosome | 2 |
| Start position | 220294783 |
| Stop position | 220294784 |
| Associated gene(s) | DES, SPEG |
| Mutation type | Tagged SNP |
| Reference | AG |
| Alternative | AGG |
| Associated allele | A |
| Associated African Allele Frequency | - |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs71040457 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Hu_rs71040457 | Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data | COVID-19 positive individuals | DES, SPEG | rs71040457 | Positive | Severe | 0.355 | 1.331 | 0.0077 |
| Paper |
|---|
| Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data |