| RSID | rs11844522 |
| HGVS | NC_000014.9:g.106066331C>T |
| Chromosome | 14 |
| Start position | 106066331 |
| Stop position | 106066331 |
| Associated gene(s) | IGHV3-7 |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | T |
| Associated allele | T |
| Associated African Allele Frequency | 0.5075 |
| Consequence | Synonymous mutation |
| Other population frequencies link | ALFA rs11844522 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| van_Blokland_rs11844522 | Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility | D1 | IGH | rs11844522 | Positive | Mild | 0.0 | None | 0.00000019 |
| van_Blokland_rs11844522 | Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility | D1 vs B2 | IGH | rs11844522 | Positive | Severe | 0.0 | None | 0.0398 |
| Paper |
|---|
| Using symptom-based case predictions to identify host genetic factors that contribute to COVID-19 susceptibility |