| RSID | rs10774671 |
| HGVS | NC_000012.12:g.112919388G>A |
| Chromosome | 12 |
| Start position | 112919388 |
| Stop position | 112919388 |
| Associated gene(s) | OAS1, OAS2, OAS3 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A/C |
| Associated allele | A |
| Associated African Allele Frequency | 0.4257 |
| Consequence | Splice acceptor variant |
| Other population frequencies link | ALFA rs10774671 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| COVID-19 HGI_rs10774671 | Mapping the human genetic architecture of COVID-19 | Hospitalised vs Controls | OAS1, OAS2, OAS3 | rs10774671 | Positive | Severe | 0.664 | 1.107 | 0.000000000614 |
| COVID-19 HGI_rs10774671 | Mapping the human genetic architecture of COVID-19 | Critical vs Controls | OAS1, OAS2, OAS3 | rs10774671 | Positive | Critical | 0.652 | 1.2 | 0.000000000000408 |
| Paper |
|---|
| Mapping the human genetic architecture of COVID-19 |