| RSID | rs155788 |
| HGVS | NC_000005.10:g.179833528T>C/G |
| Chromosome | 5 |
| Start position | 179833528 |
| Stop position | 179833528 |
| Associated gene(s) | SQSTM1 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C/G |
| Associated allele | - |
| Associated African Allele Frequency | 0.4215 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs155788 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs155788 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | SQSTM1 | rs155788 | positive | Severe | None | None | 0.0006471 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |