Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Ala1794Asp (p.A1794D)
(
ENST00000370225.4 )
ABCA4 p.Ala1794Asp (p.A1794D) ( ENST00000370225.4 ) - Associated Disease
- Retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.5381C>A (p.Ala1794Asp) AND Retinal dystrophy
- ClinVar Allele ID
- 105260
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.5381C>A
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.5159C>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-08-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000504739
- ClinVar Disease
- Retinal dystrophy
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs