"Fulgent Genetics, Fulgent Genetics"[submitter] AND "FGF12"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1548117	NM_004113.6(FGF12):c.229-8dup	FGF12	Duplication (intron variant)	Developmental and epileptic encephalopathy, 47 +1 more	GBenign/Likely benign
Select item 1392428	NM_004113.6(FGF12):c.125-3C>G	FGF12	Single nucleotide variant (intron variant)	Developmental and epileptic encephalopathy, 47 +1 more	GUncertain significance