RSID | rs151256885 |
HGVS | NC_000017.10:g.8013217C>T |
Chromosome | 17 |
Start position | 8013217 |
Stop position | 8013217 |
Associated gene(s) | ALOXE3 |
Mutation type | SNP |
Reference | C |
Alternative | G/T |
Associated allele | T |
Associated African Allele Frequency | 0.0161 |
Consequence | Intronic |
Other population frequencies link | ALFA rs151256885 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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