Annotation Detail
Information
- Associated Genes
- ITGB3
- Associated Variants
-
ITGB3 p.Leu59Pro (p.L59P)
(
ENST00000559488.7,
ENST00000571680.1,
ENST00000696963.1 )
ITGB3 p.Leu59Pro (p.L59P) ( ENST00000559488.7, ENST00000571680.1, ENST00000696963.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000212.3(ITGB3):c.176T>C (p.Leu59Pro) AND not provided
- ClinVar Allele ID
- 28597
- ClinVar RefSeq Alternation Syntax
- NM_000212.3:c.176T>C
- 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/RCV001517663
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs