| RSID | rs3766539 |
| HGVS | NC_000001.11:g.203224133T>C |
| Chromosome | 1 |
| Start position | 203224133 |
| Stop position | 203224133 |
| Associated gene(s) | CHIT1 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C |
| Associated allele | - |
| Associated African Allele Frequency | 0.0176 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs3766539 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs3766539 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | CHIT1 | rs3766539 | positive | Severe | None | None | 0.0001874 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |