Annotation Detail
Information
- Associated Genes
- GNB3 CDCA3
- Associated Variants
-
GNB3 c.700-126G>A
(
ENST00000229264.8,
ENST00000422785.7,
ENST00000435982.6 )
GNB3 c.700-126G>A ( ENST00000229264.8, ENST00000435982.6, ENST00000422785.7 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002075.4(GNB3):c.700-126G>A AND not provided
- ClinVar Allele ID
- 667211
- ClinVar RefSeq Alternation Syntax
- NM_002075.4:c.700-126G>A
- ClinVar RefSeq Alternation Syntax
- NM_001297571.2:c.697-126G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-31
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000835187
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs