Annotation Detail
Information
- Associated Genes
- HBB LOC106099062 LOC107133510
- Associated Variants
-
HBB c.-138C>G
(
ENST00000647020.1 )
HBB c.-138C>G ( ENST00000647020.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000518.4(HBB):c.-138C>G AND not provided
- ClinVar Allele ID
- 857539
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-12-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003478698
- ClinVar Disease
- not provided
- Observed Origin Sample
- unknown
Drugs