"Genome-Nilou Lab"[submitter] AND "DEAF1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1185384	NM_021008.4(DEAF1):c.1504-40C>T	DEAF1	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185385	NM_021008.4(DEAF1):c.1503+82C>A	DEAF1, LOC126861109	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185386	NM_021008.4(DEAF1):c.1503+78C>T	DEAF1, LOC126861109	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185387	NM_021008.4(DEAF1):c.1503+37C>T	DEAF1, LOC126861109	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185388	NM_021008.4(DEAF1):c.998-99C>T	DEAF1	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185389	NM_021008.4(DEAF1):c.997+97T>C	DEAF1	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185390	NM_021008.4(DEAF1):c.518-34G>A	DEAF1	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign
Select item 1185391	NM_021008.4(DEAF1):c.290-38C>T	DEAF1	Single nucleotide variant (intron variant)	Intellectual disability, autosomal dominant 24 +2 more	GBenign

ClinVar