RSID | rs2176724 |
HGVS | NC_000002.11:g.196952410G>A |
Chromosome | 2 |
Start position | 196952410 |
Stop position | 196952410 |
Associated gene(s) | DNAH7, SLC39A18 |
Mutation type | Tagged SNP |
Reference | G |
Alternative | A |
Associated allele | A |
Associated African Allele Frequency | 0.3642 |
Consequence | Intergenic |
Other population frequencies link | ALFA rs2176724 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
---|---|---|---|---|---|---|---|---|---|
Hu_rs2176724 | Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data | COVID-19 positive individuals | DNAH7, SLC39A10 | rs2176724 | Positive | Severe | 0.138 | 1.484 | 0.0061 |
Paper |
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Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data |