C5436699[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2441959	NM_014712.3(SETD1A):c.3251T>C (p.Val1084Ala)	SETD1A (V1084A)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with speech impairment and dysmorphic facies	GUncertain significance
Select item 2441734	NM_014712.3(SETD1A):c.4511A>G (p.Lys1504Arg)	SETD1A (K1504R)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with speech impairment and dysmorphic facies	GUncertain significance