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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PGAP1
(K134fs +1 more)
Deletion
(frameshift variant +1 more)
Cerebral visual impairment and intellectual disability
GPathogenic
PGAP1
(P92del)
Deletion
(5 prime UTR variant +1 more)
Cerebral visual impairment and intellectual disability
GPathogenic