| RSID | rs884811 |
| HGVS | NC_000010.10:g.99923763C>G |
| Chromosome | 10 |
| Start position | 99923763 |
| Stop position | 99923763 |
| Associated gene(s) | R3HCC1L |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | A/G/T |
| Associated allele | G |
| Associated African Allele Frequency | 0.0252 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs884811 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|
| Paper |
|---|