C4748195[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1332943	NM_003011.4(SET):c.132-17C>T	SET	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 58 +1 more	GBenign
Select item 1332944	NM_003011.4(SET):c.493-14C>T	SET	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 58 +1 more	GBenign