| RSID | rs3787950 |
| HGVS | NC_000021.8:g.42866296T>C |
| Chromosome | 21 |
| Start position | 41494369 |
| Stop position | 41494369 |
| Associated gene(s) | TMPRSS2 |
| Mutation type | SNP |
| Reference | T |
| Alternative | C |
| Associated allele | C |
| Associated African Allele Frequency | 0.2018 |
| Consequence | Synonymous variant |
| Other population frequencies link | ALFA rs3787950 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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