ClinVar for MedGen (Select 96906) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2571623	NM_003112.5(SP4):c.90dup (p.Asn31Ter)	SP4 (N14* +1 more)	Duplication (nonsense +2 more)	Attention deficit hyperactivity disorder +5 more	GUncertain significance
Select item 2570695	NM_001039469.3(MARK2):c.1931G>T (p.Arg644Leu)	MARK2 (R610L +3 more)	Single nucleotide variant (missense variant)	Seizure +5 more	GUncertain significance