RSID | rs1042542 |
HGVS | NC_000017.11:g.78225347T>C |
Chromosome | 17 |
Start position | 78225347 |
Stop position | 78225347 |
Associated gene(s) | BIRC5 |
Mutation type | Tagged SNP |
Reference | T |
Alternative | C |
Associated allele | - |
Associated African Allele Frequency | 0.6139 |
Consequence | Non coding transcript variant |
Other population frequencies link | ALFA rs1042542 |
Name | Paper | Description of Comparison | Gene | RSID | Association | Disease Status | MAF | Statistical Odds Ratio | Statistical P-value |
---|---|---|---|---|---|---|---|---|---|
Upadhyai_rs1042542 | Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent | Asymptomatic vs Severe cases | BIRC5 | rs1042542 | positive | Severe | None | None | 0.0004409 |
Paper |
---|
Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent |