Annotation Detail
Information
- Associated Genes
- ATOH7
- Associated Variants
-
ATOH7 c.-419T>C
(
ENST00000373673.5 )
ATOH7 c.-419T>C ( ENST00000373673.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_145178.4(ATOH7):c.-419T>C AND not provided
- ClinVar Allele ID
- 1226500
- ClinVar RefSeq Alternation Syntax
- NM_145178.4:c.-419T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001635868
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs