Annotation Detail
Information
- Associated Genes
- HAMP
- Associated Variants
-
HAMP c.-84-498A>G
(
ENST00000598398.5 )
HAMP c.-84-498A>G ( ENST00000598398.5 ) - Associated Disease
- Hereditary hemochromatosis
- Source Database
- ClinVar
- Description
- NC_000019.10:g.35281996A>G AND Hereditary hemochromatosis
- ClinVar Allele ID
- 1158503
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001517972
- ClinVar Disease
- Hereditary hemochromatosis
- Observed Origin Sample
- germline
Drugs