RS606231181 RPGR
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked cone-rod dystrophy 1
Retinal dystrophy
Retinitis pigmentosa 3
Cone dystrophy
Primary ciliary dyskinesia
RPGR-related disorder
RPGR-related retinopathy
X-linked cone-rod dystrophy 1
Retinal dystrophy
Retinitis pigmentosa 3
Cone dystrophy
Primary ciliary dyskinesia
RPGR-related disorder
RPGR-related retinopathy
Other Variants in RPGR