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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ROM1
(D210V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ROM1
(L238fs)
Deletion
(frameshift variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ROM1
(R242Q)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+1 more
GUncertain significance
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