| RSID | rs77578623 |
| HGVS | NC_000002.11:g.196369073C>T |
| Chromosome | 2 |
| Start position | 196369073 |
| Stop position | 196369073 |
| Associated gene(s) | DNAH7, SLC39A10, LOC105376755 |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | T |
| Associated allele | T |
| Associated African Allele Frequency | 0.0262 |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs77578623 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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