RSID | rs9268517 |
HGVS | NC_000006.12:g.32411963C>T |
Chromosome | 6 |
Start position | 32411963 |
Stop position | 32411963 |
Associated gene(s) | BTNL2,HLA-DRA |
Mutation type | SNP |
Reference | C |
Alternative | T |
Associated allele | T |
Associated African Allele Frequency | 0.0751 |
Consequence | Downstream transcript variant |
Other population frequencies link | ALFA rs9268517 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
---|
Paper |
---|