| RSID | rs4782327 |
| HGVS | NC_000016.10:g.89117727= |
| Chromosome | 16 |
| Start position | 89117727 |
| Stop position | 89117727 |
| Associated gene(s) | ACSF3 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A,C,T |
| Associated allele | G |
| Associated African Allele Frequency | 0.3401 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs4782327 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Horowitz_rs4782327 | Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease | Meta analysis, External data | ACSF3 | rs4782327 | Positive | Severe | 0.22 | 1.17 | 0.000000008 |
| Paper |
|---|
| Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease |