RSID | Fallerini_c.901T>C |
HGVS | GRCh38.p13 chr X_c.901T>C |
Chromosome | X |
Start position | 12867072 |
Stop position | 12890361 |
Associated gene(s) | TLR7 |
Mutation type | SNP |
Reference | - |
Alternative | - |
Associated allele | - |
Associated African Allele Frequency | - |
Consequence | Missense Variant |
Other population frequencies link | ALFA Fallerini_c.901T>C |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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Paper |
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