Annotation Detail
Information
- Associated Genes
- FOXL2
- Associated Variants
-
FOXL2 p.Tyr274Ter (p.Y274*)
(
ENST00000648323.1 )
FOXL2 p.Tyr274Ter (p.Y274*) ( ENST00000648323.1 ) - Associated Disease
- blepharophimosis, ptosis, and epicanthus inversus syndrome Premature ovarian failure 3
- Source Database
- ClinVar
- Description
- NM_023067.4(FOXL2):c.822C>G (p.Tyr274Ter) AND multiple conditions
- ClinVar Allele ID
- 19900
- ClinVar RefSeq Alternation Syntax
- NM_023067.4:c.822C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-03-29
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002496265
- ClinVar Disease
- Premature ovarian failure 3
- ClinVar Disease
- Blepharophimosis, ptosis, and epicanthus inversus syndrome
- Observed Origin Sample
- unknown
Drugs