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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PPP3CA
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
PPP3CA
(S375fs +1 more)
Deletion
(frameshift variant)
Epileptic encephalopathy, infantile or early childhood, 1
GPathogenic
PPP3CA
(H281Q)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy, infantile or early childhood, 1
GLikely pathogenic
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