| RSID | rs7305574 |
| HGVS | NC_000012.12:g.3716547T>A/C |
| Chromosome | 12 |
| Start position | 3716547 |
| Stop position | 3716547 |
| Associated gene(s) | CRACR2A |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | A/C |
| Associated allele | - |
| Associated African Allele Frequency | 0.1189 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs7305574 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs7305574 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | CRACR2A | rs7305574 | positive | Severe | None | None | 0.0006086 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |