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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRB1
(I111fs +1 more)
Deletion
(frameshift variant +1 more)
Retinitis pigmentosa 12
GLikely pathogenic
CRB1
(C948Y +2 more)
Single nucleotide variant
(missense variant +2 more)
CRB1-related disorder
+7 more
GPathogenic