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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD1A
(K1505E)
Single nucleotide variant
(missense variant)
Epilepsy, early-onset, with or without developmental delay
GUncertain significance
SETD1A
(R1610Q)
Single nucleotide variant
(missense variant)
Epilepsy, early-onset, with or without developmental delay
GUncertain significance