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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PI4KA, SERPIND1
(E74fs)
Duplication
(frameshift variant +1 more)
Heparin cofactor II deficiency
GUncertain significance
AIFM3, SNAP29
+7 more
Copy number gain
Intellectual disability, mild
+8 more
GUncertain significance
DGCR8, ESS2
+45 more
Copy number loss
Ear malformation
+13 more
GPathogenic
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