| RSID | rs1042542 |
| HGVS | NC_000017.11:g.78225347T>C |
| Chromosome | 17 |
| Start position | 78225347 |
| Stop position | 78225347 |
| Associated gene(s) | BIRC5 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C |
| Associated allele | - |
| Associated African Allele Frequency | 0.6139 |
| Consequence | Non coding transcript variant |
| Other population frequencies link | ALFA rs1042542 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs1042542 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | BIRC5 | rs1042542 | positive | Severe | None | None | 0.0004409 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |