| RSID | rs7152677 |
| HGVS | NC_000014.9:g.31953540G>C |
| Chromosome | 14 |
| Start position | 31953540 |
| Stop position | 31953540 |
| Associated gene(s) | LINC02313 |
| Mutation type | Tagged SNP |
| Reference | G |
| Alternative | C/T |
| Associated allele | C |
| Associated African Allele Frequency | 0.7476 |
| Consequence | Intergenic |
| Other population frequencies link | ALFA rs7152677 |
| Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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