C5436699[trait identifier] AND "Neuberg Centre For Genomic Medicine, N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2671656	NM_014712.3(SETD1A):c.395G>A (p.Arg132His)	SETD1A (R132H)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with speech impairment and dysmorphic facies	GUncertain significance
Select item 1339133	NM_014712.3(SETD1A):c.1787C>G (p.Pro596Arg)	SETD1A (P596R)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with speech impairment and dysmorphic facies +1 more	GUncertain significance