Annotation Detail
Information
- Associated Genes
- LEP
- Associated Variants
-
LEP p.Asn103= (p.N103=)
(
ENST00000308868.5 )
LEP p.Asn103= (p.N103=) ( ENST00000308868.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000230.3(LEP):c.309C>T (p.Asn103=) AND not provided
- ClinVar Allele ID
- 710749
- ClinVar RefSeq Alternation Syntax
- NM_000230.3:c.309C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2023-11-17
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000965438
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs