Annotation Detail
Information
- Associated Genes
- ITGA3
- Associated Variants
-
ITGA3 p.Phe332= (p.F332=)
(
ENST00000320031.13,
ENST00000007722.11 )
ITGA3 p.Phe332= (p.F332=) ( ENST00000007722.11, ENST00000320031.13 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002204.4(ITGA3):c.996C>T (p.Phe332=) AND not provided
- ClinVar Allele ID
- 1259980
- ClinVar RefSeq Alternation Syntax
- NM_002204.4:c.996C>T
- 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/RCV001681459
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs