rs2301995, ELN

N. diseases: 3
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
0.020 GeneticVariation BEFREE A statistically significant association was detected between the rs2301995 SNP and AMD (P = 0.018). 22003121 2011
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
0.020 GeneticVariation BEFREE In contrast, there were significant differences in the genotype distribution between the controls and nAMD patients only for rs2301995 (ELN, p=0.022) and rs1801133 (MTHFR, p=2.50×10(-3)). 22065928 2011