Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs644242
rs644242
0.020 GeneticVariation BEFREE Meta-analysis of existing data revealed a suggestive association of PAX6 rs644242 with extreme and high myopia, which awaits validation in further studies. 24637479

2014

dbSNP: rs644242
rs644242
0.020 GeneticVariation BEFREE After adjusting for age and sex, evaluation of cataract control showed a marginal association with high myopia in rs644242 (odds ratio [95% confidence interval]=0.69 [0.49-0.96], p=0.026), and a significant association was observed in healthy Japanese controls (0.79 [0.66-0.96], p=0.015). 23213273

2012

dbSNP: rs662702
rs662702
0.010 GeneticVariation BEFREE We showed previously that single nucleotide polymorphism (SNP) rs662702 in PAX6 may be located in a microRNA-328 binding site that causes susceptibility to high myopia. 22447870

2012

dbSNP: rs12421026
rs12421026
0.010 GeneticVariation BEFREE However, exhaustive sliding-window haplotype analysis highlighted an important role for rs12421026 because haplotypes containing this SNP were found to be associated with high myopia. 21589860

2011

dbSNP: rs3026390
rs3026390
0.010 GeneticVariation BEFREE Single marker analysis of SNPs rs3026390 and rs3026393 showed significant association with high myopia as a qualitative trait in dominant and recessive models (P = 0.0014 and P = 0.0011, respectively). 19124844

2009

dbSNP: rs3026393
rs3026393
0.010 GeneticVariation BEFREE Single marker analysis of SNPs rs3026390 and rs3026393 showed significant association with high myopia as a qualitative trait in dominant and recessive models (P = 0.0014 and P = 0.0011, respectively). 19124844

2009

dbSNP: rs667773
rs667773
0.010 GeneticVariation BEFREE Our aim was to determine whether PAX6polymorphism at position -12 of intron 9 (IVS9-12C to T, rs667773) is associated with high myopia in Chinese Taiwanese. 17948041

2008