C1970203[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 573381	NM_001003787.4(STRADA):c.992C>A (p.Thr331Asn)	STRADA (T331N +5 more)	Single nucleotide variant (missense variant +1 more)	Polyhydramnios, megalencephaly, and symptomatic epilepsy	GConflicting classifications of pathogenicity
Select item 374250	NM_001003787.4(STRADA):c.792T>A (p.Ser264Arg)	STRADA (S264R +5 more)	Single nucleotide variant (missense variant +1 more)	Polyhydramnios, megalencephaly, and symptomatic epilepsy	GUncertain significance