Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16958445
rs16958445
0.810 GeneticVariation BEFREE Meanwhile, the rs16958445 of <i>TBC1D21</i> and the rs7137828 of <i>ATXN2</i> have also shown to be associated with pathogenesis of XFS/XFG. 31192002

2019

dbSNP: rs16958445
rs16958445
G 0.810 GeneticVariation GWASDB Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310

2014

dbSNP: rs16958445
rs16958445
G 0.810 GeneticVariation GWASCAT Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310

2014

dbSNP: rs16958415
rs16958415
C 0.700 GeneticVariation GWASDB Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310

2014

dbSNP: rs4445847
rs4445847
C 0.700 GeneticVariation GWASDB Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310

2014

dbSNP: rs4886725
rs4886725
A 0.700 GeneticVariation GWASDB Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. 24938310

2014

dbSNP: rs12914489
rs12914489
0.010 GeneticVariation BEFREE Promoter region haplotypes that included the risk alleles for rs12914489, a SNP located in the distal promoter region and independently associated with ES, and rs16958477, a SNP previously shown to affect gene transcription, were associated with increased disease risk (P=0.0008; odds ratio [OR], 2.34; 95% confidence interval [CI], 1.42-3.85) and with protective effects (P=2.3 × 10(-6); OR, 0.38; 95% CI, 0.25-0.57). 21212179

2011