| RSID | rs505922 |
| HGVS | NC_000009.12:g.133273813C>T |
| Chromosome | 9 |
| Start position | 133273813 |
| Stop position | 133273813 |
| Associated gene(s) | ABO |
| Mutation type | SNV |
| Reference | C |
| Alternative | T |
| Associated allele | - |
| Associated African Allele Frequency | 0.6477 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs505922 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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