Annotation Detail

Information
Associated Genes
CFH
Associated Variants
ENSG00000289697 p.Ala473= (p.A473=), CFH p.Ala473= (p.A473=) ( ENST00000695976.1, ENST00000695970.1, ENST00000367429.9, ENST00000695974.1, ENST00000695969.1, ENST00000695971.1, ENST00000695981.1, ENST00000695984.1, ENST00000696029.1, ENST00000696027.1, ENST00000696028.1 )
ENSG00000289697 p.Ala473= (p.A473=), CFH p.Ala473= (p.A473=) ( ENST00000367429.9, ENST00000695969.1, ENST00000695970.1, ENST00000695971.1, ENST00000695974.1, ENST00000695976.1, ENST00000695981.1, ENST00000695984.1, ENST00000696027.1, ENST00000696028.1, ENST00000696029.1 )
Associated Disease
age related macular degeneration 4
Source Database
ClinVar
Description
NM_000186.4(CFH):c.1419G>C (p.Ala473=) AND Age related macular degeneration 4
ClinVar Allele ID
31595
ClinVar RefSeq Alternation Syntax
NM_000186.4:c.1419G>C
Clinical Significance Description
risk factor
Clinical Significance Last Update
2006-09-01
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000018023
ClinVar Disease
Age related macular degeneration 4
Observed Origin Sample
germline
Pubmed
16936733
Drugs