RSID | rs5874914 |
HGVS | NC_000006.12:g.23379133del |
Chromosome | 6 |
Start position | 23379133 |
Stop position | 23379133 |
Associated gene(s) | LOC102724749, LOC105374976, AL139231.1 |
Mutation type | InDel |
Reference | AT |
Alternative | A |
Associated allele | A |
Associated African Allele Frequency | 0.0024 |
Consequence | Non coding transcript variant |
Other population frequencies link | ALFA rs5874914 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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