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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1264118	NM_021738.3(SVIL):c.6133+15G>A	SVIL, SVIL-AS1	Single nucleotide variant (intron variant)	Myofibrillar myopathy 10 +1 more	GBenign/Likely benign
Select item 786582	NM_021738.3(SVIL):c.4241G>C (p.Ser1414Thr)	SVIL (S1104T +3 more)	Single nucleotide variant (missense variant)	Myofibrillar myopathy 10 +1 more	GBenign/Likely benign