| RSID | rs117928001 |
| HGVS | NC_000006.11:g.147514999C>T |
| Chromosome | 6 |
| Start position | 147514999 |
| Stop position | 147514999 |
| Associated gene(s) | STXBP5, STXBP5-AS1 |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | A/G/T |
| Associated allele | T |
| Associated African Allele Frequency | 0.0021 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs117928001 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Hu_rs117928001 | Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data | COVID-19 positive individuals | STXBP5, STXBP5-AS1 | rs117928001 | Positive | Severe | 0.049 | 2.749 | 0.000011 |
| Paper |
|---|
| Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data |