| RSID | rs34418657 |
| HGVS | NC_000003.12:g.46373293G>T |
| Chromosome | 3 |
| Start position | 46373293 |
| Stop position | 46373293 |
| Associated gene(s) | CCR5 |
| Mutation type | SNP |
| Reference | G |
| Alternative | A/T |
| Associated allele | T |
| Associated African Allele Frequency | 0 |
| Consequence | Missense Variant |
| Other population frequencies link | ALFA rs34418657 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Cantalupo_rs34418657 | Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19 | Hospitalised cases with heterozygous SNP vs control | CCR5 | rs34418657 | positive | Severe | None | None | 0.027 |
| Paper |
|---|
| Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19 |