RSID | TLR7 deletion |
HGVS | NM_016562.3:c.2129_2132del |
Chromosome | X |
Start position | 12905756 |
Stop position | 12905759 |
Associated gene(s) | TLR7 |
Mutation type | InDel |
Reference | AACT |
Alternative | - |
Associated allele | - |
Associated African Allele Frequency | none |
Consequence | Non sense |
Other population frequencies link | ALFA TLR7 deletion |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
---|
Paper |
---|