Gene: RPGR ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312185
rs869312185
RPGR
C 0.700 CausalMutation CLINVAR Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. 26872967

2016
dbSNP: rs1569235803
rs1569235803
RPGR
A 0.700 CausalMutation CLINVAR

dbSNP: rs878853374
rs878853374
RPGR
A 0.700 GeneticVariation CLINVAR