Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
BASAL LAMINAR DRUSEN (disorder)
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
0.720 GeneticVariation BEFREE In patients with CD, the association with the CFH Y402H risk allele was significantly higher (p=0.022), whereas the association with current smoking was significantly lower (p<0.001) than in the heterogeneous group of patients with "non-CD" AMD. 22933840 2012
BASAL LAMINAR DRUSEN (disorder)
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
0.720 GeneticVariation BEFREE The cuticular drusen phenotype is highly associated with the Tyr402His variant of the complement factor H (CFH) gene. 17210858 2007
BASAL LAMINAR DRUSEN (disorder)
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
0.720 CausalMutation CLINVAR