| RSID | rs2957702 |
| HGVS | NC_000011.10:g.10352760T>A/C/G |
| Chromosome | 11 |
| Start position | 10352760 |
| Stop position | 10352760 |
| Associated gene(s) | CAND1.11 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | A/C/G |
| Associated allele | - |
| Associated African Allele Frequency | 0.5545 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs2957702 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs2957702 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | CAND1.11 | rs2957702 | positive | Severe | None | None | 0.0006268 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |