Annotation Detail
Information
- Associated Genes
- OSGEP
- Associated Variants
-
OSGEP c.702+16A>G
(
ENST00000206542.9 )
OSGEP c.702+16A>G ( ENST00000206542.9 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_017807.4(OSGEP):c.702+16A>G AND not provided
- ClinVar Allele ID
- 1157191
- ClinVar RefSeq Alternation Syntax
- NM_017807.4:c.702+16A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001511841
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs