| RSID | rs10786398 |
| HGVS | NC_000010.10:g.99926570G>T |
| Chromosome | 10 |
| Start position | 99926570 |
| Stop position | 99926570 |
| Associated gene(s) | R3HCC1L |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A/C/T |
| Associated allele | T |
| Associated African Allele Frequency | 0.0068 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs10786398 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Chen_rs10786398 | Host genetic effects in Pneumonia | COVID-19 HGI severity vs contr | R3HCC1L | rs10786398 | Positive | Severe | None | 1.19 | 0.0372 |
| Paper |
|---|
| Host genetic effects in Pneumonia |