| RSID | rs6065904 |
| HGVS | NC_000020.11:g.45906012G>A |
| Chromosome | 20 |
| Start position | 45906012 |
| Stop position | 45906012 |
| Associated gene(s) | PLTP |
| Mutation type | SNV |
| Reference | G |
| Alternative | A |
| Associated allele | - |
| Associated African Allele Frequency | 0.22678 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs6065904 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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