Annotation Detail
Information
- Associated Genes
- ITGB3
- Associated Variants
-
ITGB3 p.Arg169Gln (p.R169Q)
(
ENST00000571680.1,
ENST00000559488.7,
ENST00000696963.1 )
ITGB3 p.Arg169Gln (p.R169Q) ( ENST00000559488.7, ENST00000571680.1, ENST00000696963.1 ) - Associated Disease
- PEN(a)/PEN(b) ALLOANTIGEN POLYMORPHISM
- Source Database
- ClinVar
- Description
- NM_000212.3(ITGB3):c.506G>A (p.Arg169Gln) AND PEN(a)/PEN(b) ALLOANTIGEN POLYMORPHISM
- ClinVar Allele ID
- 28596
- ClinVar RefSeq Alternation Syntax
- NM_000212.3:c.506G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 1992-11-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014516
- ClinVar Disease
- PEN(a)/PEN(b) ALLOANTIGEN POLYMORPHISM
- Observed Origin Sample
- germline
- Pubmed
- 1430225
Drugs