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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABCA4
Single nucleotide variant
(stop lost)
Cone-rod dystrophy 3
GUncertain significance
ABCA4
(Q1713R +1 more)
Indel
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic