Annotation Detail
Information
- Associated Genes
- WFS1
- Associated Variants
-
WFS1 p.Thr699Met (p.T699M)
(
ENST00000226760.5,
ENST00000503569.5,
ENST00000506362.2,
ENST00000673991.1,
ENST00000682275.1,
ENST00000684087.1 )
WFS1 p.Thr699Met (p.T699M) ( ENST00000226760.5, ENST00000503569.5, ENST00000506362.2, ENST00000673991.1, ENST00000682275.1, ENST00000684087.1 ) - Associated Disease
- Autosomal dominant nonsyndromic hearing loss 6
- Source Database
- ClinVar
- Description
- NM_006005.3(WFS1):c.2096C>T (p.Thr699Met) AND Autosomal dominant nonsyndromic hearing loss 6
- ClinVar Allele ID
- 19561
- ClinVar RefSeq Alternation Syntax
- NM_006005.3:c.2096C>T
- ClinVar RefSeq Alternation Syntax
- NM_001145853.1:c.2096C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2002-05-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000004780
- ClinVar Disease
- Autosomal dominant nonsyndromic hearing loss 6
- Observed Origin Sample
- germline
- Pubmed
- 12073007
Drugs