Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Gly11LeufsTer24 (p.G11Lfs*24)
(
ENST00000382848.5,
ENST00000382844.2 )
GJB2 p.Gly11LeufsTer24 (p.G11Lfs*24) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Autosomal dominant nonsyndromic hearing loss 3A
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.31_68del (p.Gly11fs) AND Autosomal dominant nonsyndromic hearing loss 3A
- ClinVar Allele ID
- 53905
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2016-03-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000411009
- ClinVar Disease
- Autosomal dominant nonsyndromic hearing loss 3A
- Observed Origin Sample
- unknown
Drugs