Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917745
rs121917745
RPE65
A 0.800 CausalMutation CLINVAR

dbSNP: rs61752909
rs61752909
RPE65
G 0.800 CausalMutation CLINVAR

dbSNP: rs62637004
rs62637004
RPE65
C 0.800 CausalMutation CLINVAR

dbSNP: rs62642584
rs62642584
RPE65
A 0.800 CausalMutation CLINVAR

dbSNP: rs62653011
rs62653011
RPE65
G 0.800 CausalMutation CLINVAR

dbSNP: rs1193631220
rs1193631220
RPE65
0.700 GeneticVariation UNIPROT

dbSNP: rs1266217912
rs1266217912
RPE65
0.700 GeneticVariation UNIPROT

dbSNP: rs61751276
rs61751276
RPE65
T 0.700 CausalMutation CLINVAR

dbSNP: rs61751276
rs61751276
RPE65
T 0.700 GeneticVariation CLINVAR

dbSNP: rs747393487
rs747393487
RPE65
T 0.700 CausalMutation CLINVAR

dbSNP: rs121917745
rs121917745
RPE65
0.800 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752871
rs61752871
RPE65
0.800 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752909
rs61752909
RPE65
0.800 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs62637004
rs62637004
RPE65
0.800 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs62642584
rs62642584
RPE65
0.800 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs62653011
rs62653011
RPE65
0.800 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752869
rs61752869
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752870
rs61752870
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752874
rs61752874
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752877
rs61752877
RPE65
A 0.700 CausalMutation CLINVAR Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752878
rs61752878
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752883
rs61752883
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752896
rs61752896
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs61752901
rs61752901
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998
dbSNP: rs62637002
rs62637002
RPE65
0.700 GeneticVariation UNIPROT Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis. 9501220

1998