Annotation Detail
Information
- Associated Genes
- CYP1B1
- Associated Variants
-
CYP1B1 p.Val198Ile (p.V198I)
(
ENST00000490576.2,
ENST00000494864.1,
ENST00000610745.5,
ENST00000614273.1,
ENST00000714520.1 )
CYP1B1 p.Val198Ile (p.V198I) ( ENST00000490576.2, ENST00000494864.1, ENST00000610745.5, ENST00000614273.1, ENST00000714520.1 ) - Associated Disease
- Congenital glaucoma
- Source Database
- ClinVar
- Description
- NM_000104.4(CYP1B1):c.592G>A (p.Val198Ile) AND Congenital glaucoma
- ClinVar Allele ID
- 884856
- ClinVar RefSeq Alternation Syntax
- NM_000104.4:c.592G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003758998
- ClinVar Disease
- Congenital glaucoma
- Observed Origin Sample
- germline
Drugs