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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYBA1
Single nucleotide variant
(splice donor variant)
Inborn genetic diseases
+2 more
GPathogenic
CRYBA1
(S209W)
Single nucleotide variant
(missense variant)
Cataract 10 multiple types
GLikely pathogenic