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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MEF2C
(Y173N +7 more)
Single nucleotide variant
(missense variant)
Seizure
GLikely benign
MEF2C
(R15H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity