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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TEK
(K145fs +1 more)
Deletion
(frameshift variant)
Glaucoma 3, primary congenital, E
GLikely pathogenic
TEK
(I1116T +4 more)
Single nucleotide variant
(missense variant)
Multiple cutaneous and mucosal venous malformations
GUncertain significance
GBA2, MPDZ
+195 more
Copy number gain
not provided
GPathogenic
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