| RSID | rs200553089 |
| HGVS | NM_016562.3:c.2383G>T |
| Chromosome | X |
| Start position | 12906010 |
| Stop position | 12906010 |
| Associated gene(s) | TLR7 |
| Mutation type | SNP |
| Reference | G |
| Alternative | T |
| Associated allele | T |
| Associated African Allele Frequency | none |
| Consequence | Missense Variant |
| Other population frequencies link | ALFA rs200553089 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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| Paper |
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