RSID | rs1455662 |
HGVS | NC_000004.12:g.179423719A>G |
Chromosome | 4 |
Start position | 179423719 |
Stop position | 179423719 |
Associated gene(s) | LOC105377567 |
Mutation type | Tagged SNP |
Reference | A |
Alternative | G |
Associated allele | G |
Associated African Allele Frequency | 0.4549 |
Consequence | Intergenic |
Other population frequencies link | ALFA rs1455662 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
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