rs2269336, COL1A1

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.030 GeneticVariation BEFREE Neither of the two SNPs showed significant association with high myopia (p(allelic)=0.252 for rs2075555, and p(allelic)=0.699 for rs2269336). 22219633 2011
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.030 GeneticVariation BEFREE There was no association noted between high myopia and rs2075555 (P=0.47, P(c)>0.99) and rs2269336 (P=0.40, P(c)>0.99). 18836165 2009
Severe myopia
CUI: C0271183
Disease: Severe myopia
0.030 GeneticVariation BEFREE The frequency of GGC/GGC diplotype constructed by the three SNPs (rs2075555, rs2269336, rs1107946) was significantly high (OR = 1.6) and associated with high myopia (P = 0.028, Pc< 0.084). 17557158 2007