Annotation Detail
Information
- Associated Genes
- CFH
- Associated Variants
-
ENSG00000289697 p.Thr956Met (p.T956M), CFH p.Thr956Met (p.T956M)
(
ENST00000696029.1,
ENST00000696027.1,
ENST00000696028.1,
ENST00000695976.1,
ENST00000695970.1,
ENST00000367429.9,
ENST00000695971.1,
ENST00000695974.1,
ENST00000695981.1,
ENST00000695984.1 )
ENSG00000289697 p.Thr956Met (p.T956M), CFH p.Thr956Met (p.T956M) ( ENST00000367429.9, ENST00000695970.1, ENST00000695971.1, ENST00000695974.1, ENST00000695976.1, ENST00000695981.1, ENST00000695984.1, ENST00000696027.1, ENST00000696028.1, ENST00000696029.1 ) - Associated Disease
- CFH-related disorder
- Source Database
- ClinVar
- Description
- NM_000186.4(CFH):c.2867C>T (p.Thr956Met) AND CFH-related disorder
- ClinVar Allele ID
- 279207
- ClinVar RefSeq Alternation Syntax
- NM_000186.4:c.2867C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2020-02-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004537633
- ClinVar Disease
- CFH-related disorder
- Observed Origin Sample
- germline
Drugs