| RSID | rs113892140 |
| HGVS | NC_000002.11:g.196439005G>A |
| Chromosome | 2 |
| Start position | 196439005 |
| Stop position | 196439005 |
| Associated gene(s) | SLC39A14, DNAH7, LINC01827 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A,T |
| Associated allele | A |
| Associated African Allele Frequency | 0.2383 |
| Consequence | Upstream transcript variant |
| Other population frequencies link | ALFA rs113892140 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|
| Paper |
|---|