Annotation Detail
Information
- Associated Genes
- ABCA4
- Associated Variants
-
ABCA4 p.Arg1898His (p.R1898H)
(
ENST00000370225.4 )
ABCA4 p.Arg1898His (p.R1898H) ( ENST00000370225.4 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_000350.3(ABCA4):c.5693G>A (p.Arg1898His) AND Inborn genetic diseases
- ClinVar Allele ID
- 105287
- ClinVar RefSeq Alternation Syntax
- NM_000350.3:c.5693G>A
- ClinVar RefSeq Alternation Syntax
- NM_001425324.1:c.5471G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2014-10-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000623966
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs