"PreventionGenetics, part of Exact Sciences"[submitter] AND "DAZL"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059559	NM_001351.4(DAZL):c.736-9G>A	DAZL	Single nucleotide variant (intron variant)	DAZL-related condition	GBenign
Select item 3056257	NM_001351.4(DAZL):c.571-4dup	DAZL	Duplication (intron variant)	DAZL-related condition	GBenign
Select item 3049955	NM_001351.4(DAZL):c.552G>A (p.Leu184=)	DAZL	Single nucleotide variant (synonymous variant)	DAZL-related condition	GLikely benign
Select item 3039325	NM_001351.4(DAZL):c.405T>C (p.Pro135=)	DAZL	Single nucleotide variant (synonymous variant)	DAZL-related condition	GBenign
Select item 3060713	NM_001351.4(DAZL):c.34A>G (p.Thr12Ala)	DAZL (T12A +1 more)	Single nucleotide variant (missense variant)	DAZL-related condition	GBenign
Select item 3057075	NM_001351.4(DAZL):c.3+717G>A	DAZL (C6Y)	Single nucleotide variant (missense variant +1 more)	DAZL-related condition	GBenign

ClinVar