C4310669[trait identifier] AND "Center for Genomics, Ann and Robert H. - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1530834	NM_001144967.3(NEDD4L):c.349-9del	NEDD4L	Deletion (intron variant)	Periventricular nodular heterotopia 7 +1 more	GConflicting classifications of pathogenicity
Select item 2500065	NM_001144967.3(NEDD4L):c.1107G>A (p.Thr369=)	NEDD4L	Single nucleotide variant (synonymous variant +1 more)	Periventricular nodular heterotopia 7	GUncertain significance