| RSID | rs879055593/9411378 |
| HGVS | NC_000009.12:g.133271182= |
| Chromosome | 9 |
| Start position | 133271182 |
| Stop position | 133271182 |
| Associated gene(s) | ABO |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | A/C |
| Associated allele | T |
| Associated African Allele Frequency | 0.1671 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs879055593/9411378 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Horowitz_2_rs879055593 | 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 | ABO | rs879055593/9411378 | positive | Susceptibility | 24.0 | 1.1 | 0.0000000000000000000000000000000007 |
| Paper |
|---|
| Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease |