Annotation Detail
Information
- Associated Genes
- GNPTAB
- Associated Variants
-
GNPTAB c.2715+2T>G
(
ENST00000299314.12 )
GNPTAB c.2715+2T>G ( ENST00000299314.12 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_024312.5(GNPTAB):c.2715+2T>G AND not provided
- ClinVar Allele ID
- 47662
- ClinVar RefSeq Alternation Syntax
- NM_024312.5:c.2715+2T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-10-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001588838
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs