"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF592"[g - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043504	NM_014630.3(ZNF592):c.379C>A (p.Leu127Met)	ZNF592 (L127M)	Single nucleotide variant (missense variant)	ZNF592-related disorder	GBenign
Select item 3057309	NM_014630.3(ZNF592):c.468C>T (p.Asn156=)	ZNF592	Single nucleotide variant (synonymous variant)	ZNF592-related disorder	GLikely benign
Select item 3052828	NM_014630.3(ZNF592):c.696G>A (p.Pro232=)	ZNF592	Single nucleotide variant (synonymous variant)	ZNF592-related disorder	GLikely benign
Select item 3039839	NM_014630.3(ZNF592):c.2242C>T (p.Leu748=)	ZNF592	Single nucleotide variant (synonymous variant)	ZNF592-related disorder	GLikely benign
Select item 3048272	NM_014630.3(ZNF592):c.2559G>C (p.Gln853His)	ZNF592 (Q853H)	Single nucleotide variant (missense variant)	ZNF592-related disorder	GLikely benign

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