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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 445931	NM_001320752.2(STS):c.259+8_259+10del	STS	Microsatellite (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1568807	NM_001320752.2(STS):c.383-16C>T	STS	Single nucleotide variant (intron variant)	X-linked ichthyosis with steryl-sulfatase deficiency +1 more	GBenign/Likely benign