Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123575
rs398123575
EYS
C 0.700 CausalMutation CLINVAR Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. 26872967

2016

dbSNP: rs869312188
rs869312188
PHF3 ; EYS
ACC 0.700 GeneticVariation CLINVAR Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. 26872967

2016

dbSNP: rs1435861529
rs1435861529
PHF3 ; EYS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs143994166
rs143994166
EYS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554214453
rs1554214453
EYS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs764163418
rs764163418
EYS
G 0.700 GeneticVariation CLINVAR

dbSNP: rs878853349
rs878853349
EYS
C 0.700 GeneticVariation CLINVAR

dbSNP: rs878853350
rs878853350
EYS
T 0.700 GeneticVariation CLINVAR