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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SETD1A
(S342C)
Single nucleotide variant
(missense variant)
Epilepsy, early-onset, with or without developmental delay
GUncertain significance
SETD1A
(V1084A)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and dysmorphic facies
GUncertain significance
SETD1A
(K1504R)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and dysmorphic facies
GUncertain significance
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