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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL3
(H477fs +2 more)
Microsatellite
(frameshift variant)
Pseudohypoaldosteronism type 2E
+1 more
GLikely pathogenic
CUL3
(L165fs +2 more)
Microsatellite
(frameshift variant)
Neurodevelopmental disorder with or without autism or seizures
+3 more
GPathogenic/Likely pathogenic