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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNGA3
(R277C +1 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic
CNGA3
(R283W +1 more)
Single nucleotide variant
(missense variant)
Monochromacy
+2 more
GPathogenic/Likely pathogenic
CNGA3
(R427C +1 more)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+4 more
GPathogenic
CNGA3
(F547L +1 more)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+3 more
GPathogenic/Likely pathogenic
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