Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Met93Ile (p.M93I)
(
ENST00000382848.5,
ENST00000382844.2 )
GJB2 p.Met93Ile (p.M93I) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.279G>A (p.Met93Ile) AND Autosomal recessive nonsyndromic hearing loss 1A
- ClinVar Allele ID
- 53900
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.279G>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2017-07-17
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000675160
- ClinVar Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Observed Origin Sample
- unknown
Drugs