| RSID | rs60811869 |
| HGVS | NC_000017.10:g.25590833T>C |
| Chromosome | 17 |
| Start position | 25590833 |
| Stop position | 25590833 |
| Associated gene(s) | WSB1 |
| Mutation type | Tagged SNP |
| Reference | T |
| Alternative | C |
| Associated allele | C |
| Associated African Allele Frequency | 0.0268 |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs60811869 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|
| Paper |
|---|