| RSID | rs117665206 |
| HGVS | NC_000006.11:g.159029487C>T |
| Chromosome | 6 |
| Start position | 159029487 |
| Stop position | 159029487 |
| Associated gene(s) | TMEM181 |
| Mutation type | SNP |
| Reference | C |
| Alternative | T |
| Associated allele | T |
| Associated African Allele Frequency | 0.0016 |
| Consequence | Missense Variant |
| Other population frequencies link | ALFA rs117665206 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Lu_rs117665206 | Genetic risk factors for death with SARS-CoV-2 from the UK Biobank | COVID Death cases vs no death | TMEM181 | rs117665206 | Positive | Critical | None | None | 0.0 |
| Paper |
|---|
| Genetic risk factors for death with SARS-CoV-2 from the UK Biobank |