Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 c.1760+2T>G
(
ENST00000370225.4,
ENST00000649773.1 )
ABCA4 c.1760+2T>G ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- Severe early-childhood-onset retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.1760+2T>G AND Severe early-childhood-onset retinal dystrophy
- ClinVar Allele ID
- 104965
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.1760+2T>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000132587
- ClinVar Disease
- Severe early-childhood-onset retinal dystrophy
- Observed Origin Sample
- not provided
Drugs