| RSID | rs12796811 |
| HGVS | NC_000011.10:g.5670244C>G |
| Chromosome | 11 |
| Start position | 5670244 |
| Stop position | 5670244 |
| Associated gene(s) | TRIM5 |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | G/T |
| Associated allele | G |
| Associated African Allele Frequency | 0.1386 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs12796811 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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