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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRX
(R41W)
Single nucleotide variant
(missense variant)
Leber congenital amaurosis 7
+4 more
GPathogenic
CRX
(Q175fs)
Microsatellite
(frameshift variant)
Leber congenital amaurosis 7
GPathogenic