Annotation Detail
Information
- Associated Genes
- MUC5B
- Associated Variants
-
MUC5B c.-3133G>T
MUC5B c.-3133G>T - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002458.2(MUC5B):c.-3133G>T AND not provided
- ClinVar Allele ID
- 39082
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2022-08-01
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002292458
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs