Annotation Detail
Information
- Associated Genes
- H1-2 H1-6 H2BC3 H1-1 HFE H2AC4 H2BC4 H3C1 H3C3 H3C2 H4C1 H4C3 H4C2 HFE-AS1 LOC121740647 LINC02980 LOC129996001 LOC129996002 LOC129996003 LOC129996004 LOC129996005 LOC129996006 LOC129996007 LOC129996008 LOC129996009 LOC129996010 LOC129996011 LOC129996012 LOC129996013 LOC129996014 LOC129996015 LOC129996016
- Associated Variants
-
GRCh38/hg38 6p22.2(chr6:25991391-26116829)x3
GRCh38/hg38 6p22.2(chr6:25991391-26116829)x3 - Source Database
- ClinVar
- Description
- GRCh38/hg38 6p22.2(chr6:25991391-26116829)x3 AND See cases
- ClinVar Allele ID
- 162159
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2011-04-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000140950
- Observed Origin Sample
- not provided
Drugs