Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894833
rs104894833
0.010 GeneticVariation BEFREE In addition, our results underscore the high prevalence of not only undiagnosed Fabry patients but functional variants of p.E66Q among the ESRD population. 22695894

2012

dbSNP: rs28935197
rs28935197
0.010 GeneticVariation BEFREE An atypical p.N215S variant of Fabry disease with end-stage renal failure. 30023289

2018