Annotation Detail
Information
- Associated Genes
- ARMS2
- Associated Variants
-
ARMS2 c.297+881C>T
(
ENST00000528446.1 )
ARMS2 c.297+881C>T ( ENST00000528446.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001099667.3(ARMS2):c.297+881C>T AND not provided
- ClinVar Allele ID
- 171884
- ClinVar RefSeq Alternation Syntax
- NM_001099667.3:c.297+881C>T
- Clinical Significance Description
- not provided
- Clinical Significance Review Status
- no assertion provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000190308
- ClinVar Disease
- not provided
- Observed Origin Sample
- not provided
Drugs