rs1410996, CFH

N. diseases: 11
Disease: Glycogen storage disease type II ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
0.030 GeneticVariation BEFREE CFH (rs1410996), HTRA1 (rs112000638) and ARMS2 (rs10490923) gene polymorphisms are associated with AMD risk in Spanish patients. 23534868 2014
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
0.030 GeneticVariation BEFREE The data suggest that the noncoding variant rs1410996 of the CFH gene moderately increased the risk of exudative AMD in a Chinese population. 19850835 2010
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
0.030 GeneticVariation BEFREE The interaction analysis between gene and environmental factors showed that smoking synergistically increased susceptibility of AMD for heterozygotes of rs1410996, with OR(interaction) of 7.33 (P(interaction) = 0.029). 19187590 2008