"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC130062568"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1581459	NM_001144967.3(NEDD4L):c.48+11C>G	LOC130062568, NEDD4L	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1637451	NM_001144967.3(NEDD4L):c.48+14C>T	LOC130062568, NEDD4L	Single nucleotide variant (intron variant)	Periventricular nodular heterotopia 7 +1 more	GBenign/Likely benign
Select item 1598162	NM_001144967.3(NEDD4L):c.48+14C>A	LOC130062568, NEDD4L	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign

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