Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568019012
rs1568019012
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569518070
rs1569518070
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1569548274
rs1569548274
T 0.700 CausalMutation CLINVAR

dbSNP: rs28934907
rs28934907
A 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
A 0.700 CausalMutation CLINVAR

dbSNP: rs28940881
rs28940881
G 0.700 CausalMutation CLINVAR

dbSNP: rs387907141
rs387907141
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507478
rs397507478
A 0.700 GeneticVariation CLINVAR

dbSNP: rs533297350
rs533297350
T 0.700 GeneticVariation CLINVAR

dbSNP: rs543860009
rs543860009
A 0.700 CausalMutation CLINVAR

dbSNP: rs569681869
rs569681869
G 0.700 GeneticVariation CLINVAR

dbSNP: rs587777893
rs587777893
A 0.700 CausalMutation CLINVAR

dbSNP: rs61754381
rs61754381
A 0.700 CausalMutation CLINVAR

dbSNP: rs61816761
rs61816761
A 0.700 CausalMutation CLINVAR

dbSNP: rs752134549
rs752134549
T 0.700 GeneticVariation CLINVAR

dbSNP: rs755604487
rs755604487
A 0.700 GeneticVariation CLINVAR

dbSNP: rs770374710
rs770374710
TG 0.700 CausalMutation CLINVAR

dbSNP: rs864321670
rs864321670
T 0.700 CausalMutation CLINVAR

dbSNP: rs866294686
rs866294686
T 0.700 GeneticVariation CLINVAR

dbSNP: rs876657380
rs876657380
C 0.700 CausalMutation CLINVAR

dbSNP: rs876657731
rs876657731
T 0.700 CausalMutation CLINVAR

dbSNP: rs878854378
rs878854378
A 0.700 GeneticVariation CLINVAR

dbSNP: rs879255531
rs879255531
T 0.700 CausalMutation CLINVAR

dbSNP: rs886041091
rs886041091
G 0.700 GeneticVariation CLINVAR

dbSNP: rs104894910
rs104894910
NYX
0.010 GeneticVariation BEFREE The c.281G>C mutation cosegregated with nyctalopia and myopia. 16670814

2006