| RSID | rs4800182 |
| HGVS | NC_000018.10:g.24233008A>G/T |
| Chromosome | 18 |
| Start position | 24233008 |
| Stop position | 24233008 |
| Associated gene(s) | OSBPL1A |
| Mutation type | Tagged SNP |
| Reference | A |
| Alternative | G/T |
| Associated allele | - |
| Associated African Allele Frequency | 0.3125 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs4800182 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs4800182 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | OSBPL1A | rs4800182 | positive | Severe | None | None | 0.0009208 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |