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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1644449	NM_015693.4(INTU):c.683-16G>C	INTU	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 780934	NM_015693.4(INTU):c.1450-9T>G	INTU	Single nucleotide variant (intron variant)	Short-rib thoracic dysplasia 20 with polydactyly +2 more	GBenign/Likely benign