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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYGS
(S167C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CRYGS
(R146C)
Single nucleotide variant
(missense variant)
Cataract 20 multiple types
GUncertain significance
CRYGS
Indel
(missense variant)
Developmental cataract
GPathogenic
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