| RSID | rs200008298 |
| HGVS | NC_000002.11:g.196602159_196602163dup |
| Chromosome | 2 |
| Start position | 196602155 |
| Stop position | 196602161 |
| Associated gene(s) | SLC39A15, DNAH7, LOC107985972 |
| Mutation type | Tagged SNP |
| Reference | A |
| Alternative | CTATA |
| Associated allele | CTATA |
| Associated African Allele Frequency | 0.0202 |
| Consequence | 3 Prime UTR Variant |
| Other population frequencies link | ALFA rs200008298 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|
| Paper |
|---|