Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Arg143Trp (p.R143W)
(
ENST00000382844.2,
ENST00000382848.5 )
GJB2 p.Arg143Trp (p.R143W) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.427C>T (p.Arg143Trp) AND Autosomal recessive nonsyndromic hearing loss 1A
- ClinVar Allele ID
- 32048
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.427C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2019-12-24
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000018533
- ClinVar Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Observed Origin Sample
- germline
- Observed Origin Sample
- inherited
- Observed Origin Sample
- unknown
- Pubmed
- 9471561
- Pubmed
- 12457154
Drugs