Annotation Detail
Information
- Associated Genes
- MYH7
- Associated Variants
-
MYH7 c.1888+1G>A
(
ENST00000713769.1,
ENST00000355349.4,
ENST00000713768.1 )
MYH7 c.1888+1G>A ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.1888+1G>A AND not provided
- ClinVar Allele ID
- 178676
- ClinVar RefSeq Alternation Syntax
- NM_001407004.1:c.1888+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.1888+1G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2017-01-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000505763
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs