| RSID | rs190509934 |
| HGVS | NC_000023.11:g.15602217T>C |
| Chromosome | X |
| Start position | 15602217 |
| Stop position | 15602217 |
| Associated gene(s) | ACE2 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C |
| Associated allele | C |
| Associated African Allele Frequency | 0.0131 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs190509934 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Horowitz_2_rs190509934 | Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease | COVID-19 positive vs COVID-19 negative or unknown | ACE2 | rs190509934 | negative | Susceptibility | 0.3 | 0.6 | 0.00000000000045 |
| Paper |
|---|
| Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease |