Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Arg184Gln (p.R184Q)
(
ENST00000382844.2,
ENST00000382848.5 )
GJB2 p.Arg184Gln (p.R184Q) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Nonsyndromic genetic hearing loss
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.551G>A (p.Arg184Gln) AND Nonsyndromic genetic hearing loss
- ClinVar Allele ID
- 38617
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.551G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-08-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002281716
- ClinVar Disease
- Nonsyndromic genetic hearing loss
- Observed Origin Sample
- germline
Drugs