| RSID | rs9411378 |
| HGVS | NC_000009.12:g.133270015A>C |
| Chromosome | 9 |
| Start position | 133270015 |
| Stop position | 133270015 |
| Associated gene(s) | ABO |
| Mutation type | Tagged SNP |
| Reference | A |
| Alternative | C/T |
| Associated allele | C |
| Associated African Allele Frequency | 0.486 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs9411378 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| Horowitz_rs9411378 | Common genetic variants identify therapeutic targets for COVID-19 and individuals at high risk of severe disease | Meta analysis, External data | ABO | rs9411378 | Positive | Susceptibility | 0.23 | 1.12 | 0.0000000006 |
| Shelton_rs9411378 | Trans-ancestry analysis reveals genetic and non-genetic associations with COVID-19 susceptibility and severity | COVID-19 positive vs COVID-19 | ABO | rs9411378 | Negative | Susceptibility | None | 0.857 | 0.000000000000000000053 |