Annotation Detail
Information
- Associated Genes
- TNFRSF1A
- Associated Variants
-
TNFRSF1A c.-610T>G
TNFRSF1A c.-610T>G - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001065.3(TNFRSF1A):c.-610T>G AND not provided
- ClinVar Allele ID
- 667205
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-19
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000834974
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs