Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Val989Ala (p.V989A)
(
ENST00000370225.4 )
ABCA4 p.Val989Ala (p.V989A) ( ENST00000370225.4 ) - Associated Disease
- Severe early-childhood-onset retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.2966T>C (p.Val989Ala) AND Severe early-childhood-onset retinal dystrophy
- ClinVar Allele ID
- 105069
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.2744T>C
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.2966T>C
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2015-01-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000504904
- ClinVar Disease
- Severe early-childhood-onset retinal dystrophy
- Observed Origin Sample
- unknown
Drugs