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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYGD, LOC100507443
(D97V)
Single nucleotide variant
(missense variant)
Cataract 4 multiple types
GUncertain significance
CRYGD, LOC100507443
(P24T)
Single nucleotide variant
(missense variant)
Aculeiform cataract
+2 more
GPathogenic/Likely pathogenic