Annotation Detail
Information
- Associated Genes
- MYH7
- Associated Variants
-
MYH7 p.Arg237Trp (p.R237W)
(
ENST00000713769.1,
ENST00000355349.4,
ENST00000713768.1 )
MYH7 p.Arg237Trp (p.R237W) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- hypertrophic cardiomyopathy
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.709C>T (p.Arg237Trp) AND Hypertrophic cardiomyopathy
- ClinVar Allele ID
- 52268
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.709C>T
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-12-16
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000811971
- ClinVar Disease
- Hypertrophic cardiomyopathy
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs