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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDE6C
(R29W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PDE6C
(G34E)
Single nucleotide variant
(missense variant)
Cone dystrophy 4
+2 more
GUncertain significance
PDE6C
(R102W)
Single nucleotide variant
(missense variant)
Achromatopsia
+1 more
GUncertain significance
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