"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF589"[g - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059438	NM_016089.3(ZNF589):c.34A>G (p.Thr12Ala)	LOC112935945, ZNF589 (T12A)	Single nucleotide variant (missense variant)	ZNF589-related disorder	GBenign
Select item 728323	NM_016089.3(ZNF589):c.96+9G>A	ZNF589	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 3059949	NM_016089.3(ZNF589):c.647C>G (p.Thr216Arg)	ZNF589 (T216R)	Single nucleotide variant (missense variant)	ZNF589-related disorder	GBenign
Select item 791241	NM_016089.3(ZNF589):c.763C>T (p.Arg255Ter)	ZNF589 (R255*)	Single nucleotide variant (nonsense)	ZNF589-related disorder +1 more	GLikely benign
Select item 3045016	NM_016089.3(ZNF589):c.874C>T (p.Arg292Cys)	ZNF589 (R292C)	Single nucleotide variant (missense variant)	ZNF589-related disorder	GLikely benign

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