Annotation Detail
Information
- Associated Genes
- COL6A1
- Associated Variants
-
COL6A1 c.957+2T>C
(
ENST00000361866.8 )
COL6A1 c.957+2T>C ( ENST00000361866.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001848.3(COL6A1):c.957+2T>C AND not provided
- ClinVar Allele ID
- 191203
- ClinVar RefSeq Alternation Syntax
- NM_001848.3:c.957+2T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2014-08-06
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000174303
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs