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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATOH7
(A59V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATOH7
(A59T)
Single nucleotide variant
(missense variant)
Foveal hypoplasia
+1 more
GPathogenic
LOC130064709, OPA3
(G15R)
Single nucleotide variant
(missense variant)
Foveal hypoplasia
GUncertain significance
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