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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1606190	NM_015331.3(NCSTN):c.437-12C>G	NCSTN	Single nucleotide variant (intron variant)	Acne inversa, familial, 1 +1 more	GLikely benign
Select item 1167236	NM_015331.3(NCSTN):c.1101+13T>C	NCSTN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1170163	NM_015331.3(NCSTN):c.1249A>T (p.Asn417Tyr)	NCSTN (N279Y +2 more)	Single nucleotide variant (missense variant)	NCSTN-related disorder +2 more	GBenign/Likely benign

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