Annotation Detail
Information
- Associated Genes
- LPL
- Associated Variants
-
LPL c.1322+483T>G
LPL c.1322+483T>G - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000237.3(LPL):c.1322+483T>G AND not provided
- ClinVar Allele ID
- 1155943
- ClinVar RefSeq Alternation Syntax
- NM_000237.3:c.1322+483T>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001513263
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs