"GeneDx"[submitter] AND "ODAD4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 1243571	NM_031421.5(ODAD4):c.246+15G>A	ODAD4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281886	NM_031421.5(ODAD4):c.651C>T (p.Gly217=)	ODAD4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1183645	NM_031421.5(ODAD4):c.1145+140del	ODAD4	Deletion (intron variant)	not provided	GBenign
Select item 1228777	NM_031421.5(ODAD4):c.1443+145del	ODAD4	Deletion (intron variant)	not provided	GBenign
Select item 1227658	NM_031421.5(ODAD4):c.1529-194C>T	ODAD4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242698	NM_031421.5(ODAD4):c.1529-192C>G	ODAD4	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar