RSID | rs190509934 |
HGVS | NC_000023.11:g.15602217T>C |
Chromosome | X |
Start position | 15602217 |
Stop position | 15602217 |
Associated gene(s) | ACE2 |
Mutation type | Tagged SNP |
Reference | T |
Alternative | C |
Associated allele | C |
Associated African Allele Frequency | 0.0131 |
Consequence | Intronic |
Other population frequencies link | ALFA rs190509934 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
---|---|---|---|---|---|---|---|---|---|
Horowitz_2_rs190509934 | Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease | COVID-19 positive vs COVID-19 negative or unknown | ACE2 | rs190509934 | negative | Susceptibility | 0.3 | 0.6 | 0.00000000000045 |
Paper |
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Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease |