| RSID | rs1819040 |
| HGVS | NC_000017.11:g.46142465T>A |
| Chromosome | 17 |
| Start position | 46142465 |
| Stop position | 46142465 |
| Associated gene(s) | KANSL1, ARHGAP27, PLEKHM1, LINC02210-CRHR1, CRHR1, SPPL2C, MAPT, STH, LRRC37A, ARL17B, LRRC37A2, ARL17A, NSF, WNT3 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | A/C/G |
| Associated allele | A |
| Associated African Allele Frequency | 0.0051 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs1819040 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|---|---|---|---|---|---|---|---|---|
| COVID-19 HGI_rs1819040 | Mapping the human genetic architecture of COVID-19 | Hospitalised vs Controls | KANSL1, ARHGAP27, PLEKHM1, LINC02210-CRHR1, CRHR1, SPPL2C, MAPT, STH, LRRC37A, ARL17B, LRRC37A2, ARL17A, NSF, WNT3 | rs1819040 | Negative | Severe | 0.186 | 0.879 | 0.000000000183 |
| Paper |
|---|
| Mapping the human genetic architecture of COVID-19 |