| RSID | rs117217714 |
| HGVS | NC_000017.10:g.25987181T>C |
| Chromosome | 17 |
| Start position | 25987181 |
| Stop position | 25987181 |
| Associated gene(s) | WSB1, LGALS9, KSR1, NOS2, LYRM9 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C |
| Associated allele | C |
| Associated African Allele Frequency | 0.0031 |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs117217714 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Hu_rs117217714 | Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data | COVID-19 positive individuals | WSB1, LGALS9, KSR1, NOS2, LYRM9 | rs117217714 | Positive | Severe | 0.013 | 6.255 | 0.000033 |
| Paper |
|---|
| Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data |