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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRX
(R41W)
Single nucleotide variant
(missense variant)
Cone-rod dystrophy
+4 more
GPathogenic
CRX
(D65H)
Single nucleotide variant
(missense variant)
Retinal dystrophy
GLikely pathogenic
CRX
(G122D)
Single nucleotide variant
(missense variant)
not specified
+6 more
GBenign/Likely benign
CRX
(L299F)
Single nucleotide variant
(missense variant)
Retinal dystrophy
GBenign
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