Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894927
rs104894927
RP2
T 0.700 CausalMutation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019

dbSNP: rs137852284
rs137852284
RP2
T 0.700 CausalMutation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019

dbSNP: rs1556318627
rs1556318627
RP2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1556318633
rs1556318633
RP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs797044561
rs797044561
RP2
C 0.700 CausalMutation CLINVAR