Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Arg2030Gln (p.R2030Q)
(
ENST00000370225.4 )
ABCA4 p.Arg2030Gln (p.R2030Q) ( ENST00000370225.4 ) - Associated Disease
- Severe early-childhood-onset retinal dystrophy cone-rod dystrophy 3 age related macular degeneration 2 retinitis pigmentosa 19
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.6089G>A (p.Arg2030Gln) AND multiple conditions
- ClinVar Allele ID
- 105317
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.6089G>A
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.5867G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-12-15
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000763436
- ClinVar Disease
- Age related macular degeneration 2
- ClinVar Disease
- Severe early-childhood-onset retinal dystrophy
- ClinVar Disease
- Cone-rod dystrophy 3
- ClinVar Disease
- Retinitis pigmentosa 19
- Observed Origin Sample
- unknown
Drugs