Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3426
Gene Symbol: CFI
CFI 		0.300 GermlineCausalMutation disease ORPHANET Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration. 25986072 2015
Entrez Id: 2202
Gene Symbol: EFEMP1
EFEMP1 		0.300 GermlineCausalMutation disease ORPHANET A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family. 19850834 2010
Entrez Id: 3075
Gene Symbol: CFH
CFH 		0.300 GermlineCausalMutation disease ORPHANET Basal laminar drusen caused by compound heterozygous variants in the CFH gene. 18252232 2008