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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH1
(T626I +1 more)
Single nucleotide variant
(missense variant)
Zimmermann-Laband syndrome 1
GUncertain significance
KCNH1
(R573C +1 more)
Single nucleotide variant
(missense variant)
Zimmermann-Laband syndrome 1
GUncertain significance
EIF2D, LPGAT1
+75 more
Copy number loss
Global developmental delay
+2 more
GPathogenic
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