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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPHA2
(I904V +1 more)
Single nucleotide variant
(missense variant)
Cataract 6 multiple types
GUncertain significance
EPHA2
(V116M +1 more)
Single nucleotide variant
(missense variant)
Cataract 6 multiple types
GUncertain significance