Annotation Detail
Information
- Associated Genes
- CFH
- Associated Variants
-
ENSG00000289697 c.3580+12G>T, CFH p.Glu1198Ter (p.E1198*)
(
ENST00000695971.1,
ENST00000695974.1,
ENST00000695976.1,
ENST00000367429.9,
ENST00000695970.1,
ENST00000695984.1,
ENST00000695981.1,
ENST00000696027.1,
ENST00000696029.1,
ENST00000696028.1 )
ENSG00000289697 c.3580+12G>T, CFH p.Glu1198Ter (p.E1198*) ( ENST00000367429.9, ENST00000695970.1, ENST00000695971.1, ENST00000695974.1, ENST00000695976.1, ENST00000695981.1, ENST00000695984.1, ENST00000696027.1, ENST00000696028.1, ENST00000696029.1 ) - Associated Disease
- Hemolytic uremic syndrome, atypical, susceptibility to, 1
- Source Database
- ClinVar
- Description
- NM_000186.4(CFH):c.3592G>T (p.Glu1198Ter) AND Hemolytic uremic syndrome, atypical, susceptibility to, 1
- ClinVar Allele ID
- 31602
- ClinVar RefSeq Alternation Syntax
- NM_000186.4:c.3592G>T
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2008-06-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000018031
- ClinVar Disease
- Hemolytic uremic syndrome, atypical, susceptibility to, 1
- Observed Origin Sample
- germline
- Pubmed
- 18268093
Drugs