Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Arg572Pro (p.R572P)
(
ENST00000649773.1,
ENST00000370225.4 )
ABCA4 p.Arg572Pro (p.R572P) ( ENST00000370225.4, ENST00000649773.1 ) - Associated Disease
- Retinal dystrophy
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.1715G>C (p.Arg572Pro) AND Retinal dystrophy
- ClinVar Allele ID
- 104962
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.1715G>C
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.1715G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-04-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001074238
- ClinVar Disease
- Retinal dystrophy
- Observed Origin Sample
- germline
Drugs