| RSID | rs2271616 |
| HGVS | NC_000003.12:g.45796521G>T |
| Chromosome | 3 |
| Start position | 45796521 |
| Stop position | 45796521 |
| Associated gene(s) | SLC6A20, CCR3, LOC107986082 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A/T |
| Associated allele | T |
| Associated African Allele Frequency | 0.0230 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs2271616 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| COVID-19 HGI_rs2271616 | Mapping the human genetic architecture of COVID-19 | Susceptibility vs Control | SLC6A20, CCR3, LOC107986082 | rs2271616 | Positive | Mild | 0.118 | 1.155 | 0.000000000000000000000000000000000179 |
| Paper |
|---|
| Mapping the human genetic architecture of COVID-19 |