| RSID | rs2176724 |
| HGVS | NC_000002.11:g.196952410G>A |
| Chromosome | 2 |
| Start position | 196952410 |
| Stop position | 196952410 |
| Associated gene(s) | DNAH7, SLC39A18 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A |
| Associated allele | A |
| Associated African Allele Frequency | 0.3642 |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs2176724 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Hu_rs2176724 | Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data | COVID-19 positive individuals | DNAH7, SLC39A10 | rs2176724 | Positive | Severe | 0.138 | 1.484 | 0.0061 |
| Paper |
|---|
| Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data |