RS398122960 RPGR
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What This Variant Does
"CLNSIG=5
Associated Conditions
Retinitis pigmentosa 3
Inborn genetic diseases
Retinitis pigmentosa
Retinal dystrophy
Primary ciliary dyskinesia
X-linked cone-rod dystrophy 1
X-linked
and sinorespiratory infections
with or without deafness
Macular degeneration
X-linked atrophic
Retinal disorder
High myopia
early-onset
RPGR-related retinopathy
Other Variants in RPGR