| RSID | rs6490100 |
| HGVS | NC_000012.12:g.116946357T>C |
| Chromosome | 12 |
| Start position | 116946357 |
| Stop position | 116946357 |
| Associated gene(s) | FBXW8 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C |
| Associated allele | - |
| Associated African Allele Frequency | 0.0393 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs6490100 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs6490100 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | FBXW8 | rs6490100 | positive | Severe | None | None | 0.0001062 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |