Annotation Detail
Information
- Associated Genes
- TNF
- Associated Variants
-
NC_000006.12:g.31575324G>A
NC_000006.12:g.31575324G>A - Associated Disease
- Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR5
- Source Database
- ClinVar
- Description
- NC_000006.12:g.31575324G>A AND Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR5
- ClinVar Allele ID
- 1036919
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-08-07
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001836995
- ClinVar Disease
- Susceptibility to severe coronavirus disease (COVID-19) due to high plasma levels of TNF, TNFR, and/or TNFR5
- Observed Origin Sample
- germline
Drugs