| RSID | rs2285666 |
| HGVS | NC_000023.10:g.15610348C>A |
| Chromosome | X |
| Start position | 15592225 |
| Stop position | 15592225 |
| Associated gene(s) | ACE2 |
| Mutation type | SNP |
| Reference | C |
| Alternative | A,G,T |
| Associated allele | A |
| Associated African Allele Frequency | 0.2315 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs2285666 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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