| RSID | rs13334749 |
| HGVS | NC_000016.10:g.4902193C>T |
| Chromosome | 16 |
| Start position | 4902193 |
| Stop position | 4902193 |
| Associated gene(s) | PPL |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | T |
| Associated allele | - |
| Associated African Allele Frequency | 0.3791 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs13334749 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs13334749 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | PPL | rs13334749 | positive | Severe | None | None | 0.0007448 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |