Annotation Detail
Information
- Associated Genes
- LEP LOC106728418
- Associated Variants
-
LEP c.-39G>A
(
ENST00000308868.5 )
LEP c.-39G>A ( ENST00000308868.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000230.3(LEP):c.-39G>A AND not provided
- ClinVar Allele ID
- 301785
- ClinVar RefSeq Alternation Syntax
- NM_000230.3:c.-39G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-12-21
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001636988
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs