| RSID | rs113827944 |
| HGVS | NC_000007.13:g.117299434G>A |
| Chromosome | 7 |
| Start position | 117299434 |
| Stop position | 117299434 |
| Associated gene(s) | CFTR |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | A |
| Associated allele | A |
| Associated African Allele Frequency | 0.002 |
| Consequence | Intronic |
| Other population frequencies link | ALFA rs113827944 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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