| RSID | rs7007951 |
| HGVS | NC_000008.10:g.98146644C>T |
| Chromosome | 8 |
| Start position | 98146644 |
| Stop position | 98146644 |
| Associated gene(s) | CPQ, LOC101927066 |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | A/T |
| Associated allele | T |
| Associated African Allele Frequency | 0.3197 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs7007951 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
|---|
| Paper |
|---|