| RSID | rs17142392 |
| HGVS | NC_000006.12:g.6626750A>C/G/T |
| Chromosome | 6 |
| Start position | 6626750 |
| Stop position | 6626750 |
| Associated gene(s) | LY86 |
| Mutation type | Tagged SNP |
| Reference | A |
| Alternative | C/G/T |
| Associated allele | - |
| Associated African Allele Frequency | 0.2623 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs17142392 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Upadhyai_rs17142392 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | LY86 | rs17142392 | positive | Severe | None | None | 0.0008216 |
| Paper |
|---|
| Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |