Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Arg1300Gln (p.R1300Q)
(
ENST00000370225.4 )
ABCA4 p.Arg1300Gln (p.R1300Q) ( ENST00000370225.4 ) - Associated Disease
- Stargardt Disease, Recessive
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.3899G>A (p.Arg1300Gln) AND Stargardt Disease, Recessive
- ClinVar Allele ID
- 105135
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.3677G>A
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.3899G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2016-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000378686
- ClinVar Disease
- Stargardt Disease, Recessive
- Observed Origin Sample
- germline
Drugs