Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501181
rs1060501181
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555966699
rs1555966699
T 0.700 GeneticVariation CLINVAR

dbSNP: rs62638634
rs62638634
A 0.700 CausalMutation CLINVAR Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa. 9399904

1997

dbSNP: rs62638634
rs62638634
A 0.700 CausalMutation CLINVAR X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60. 9855162

1998

dbSNP: rs62638634
rs62638634
A 0.700 CausalMutation CLINVAR X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function. 10937588

2000