Gene: RPGR ×
Source: CLINVAR ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.800 CausalMutation disease CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709 2019
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.800 CausalMutation disease CLINVAR A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. 11992260 2002
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.800 GeneticVariation disease CLINVAR A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. 11992260 2002
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.800 CausalMutation disease CLINVAR Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. 10932196 2000
Entrez Id: 6103
Gene Symbol: RPGR
RPGR 		0.800 GeneticVariation disease CLINVAR Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa. 10932196 2000