Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Asp1532Asn (p.D1532N)
(
ENST00000370225.4 )
ABCA4 p.Asp1532Asn (p.D1532N) ( ENST00000370225.4 ) - Associated Disease
- Retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.4594G>A (p.Asp1532Asn) AND Retinal dystrophy
- ClinVar Allele ID
- 105193
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.4594G>A
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.4372G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-05-27
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001074286
- ClinVar Disease
- Retinal dystrophy
- Observed Origin Sample
- germline
Drugs