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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYBB2
(C38R)
Single nucleotide variant
(missense variant)
Cataract 3 multiple types
GUncertain significance
CRYBB2
(S51F)
Single nucleotide variant
(missense variant)
Cataract 3 multiple types
GUncertain significance
CRYBB2
(G161R)
Single nucleotide variant
(missense variant)
Cataract 3 multiple types
GUncertain significance
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