Annotation Detail
Information
- Associated Genes
- TNF
- Associated Variants
-
TNF c.-488G>A
TNF c.-488G>A - Associated Disease
- Susceptibility to severe coronavirus disease (COVID-19)
- Source Database
- ClinVar
- Description
- NM_000594.3(TNF):c.-488G>A AND Susceptibility to severe coronavirus disease (COVID-19)
- ClinVar Allele ID
- 227757
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2021-02-09
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001354056
- ClinVar Disease
- Susceptibility to severe coronavirus disease (COVID-19)
- Observed Origin Sample
- germline
Drugs