| RSID | rs7086391 |
| HGVS | NC_000010.10:g.100013563C>T |
| Chromosome | 10 |
| Start position | 100013563 |
| Stop position | 100013563 |
| Associated gene(s) | R3HCC1L/LOXL4 |
| Mutation type | Tagged SNP |
| Reference | C |
| Alternative | T |
| Associated allele | T |
| Associated African Allele Frequency | 0.1623 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs7086391 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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