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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LDLR
(G592E +3 more)
Single nucleotide variant
(missense variant)
Hypercholesterolemia, familial, 1
GPathogenic
CASK
(N643fs +2 more)
Duplication
(frameshift variant)
Syndromic X-linked intellectual disability Najm type
GPathogenic