| RSID | rs12461764 |
| HGVS | NC_000019.10:g.51739497= |
| Chromosome | 19 |
| Start position | 51739497 |
| Stop position | 51739497 |
| Associated gene(s) | FPR1, HAS1 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A,C,T |
| Associated allele | G |
| Associated African Allele Frequency | 0.2417 |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs12461764 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Horowitz_rs12461764 | Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease | Meta analysis, External data | FPR1, HAS1 | rs12461764 | Positive | Severe | 0.35 | 1.18 | 0.00000001 |
| Paper |
|---|
| Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease |