RSID | rs55986907 |
HGVS | NC_000007.13:g.22817292C>T |
Chromosome | 7 |
Start position | 22817292 |
Stop position | 22817292 |
Associated gene(s) | TOMM7, IL-6 |
Mutation type | Tagged SNP |
Reference | C |
Alternative | A/T |
Associated allele | T |
Associated African Allele Frequency | 0.1494 |
Consequence | Intergenic |
Other population frequencies link | ALFA rs55986907 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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