"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZNF668"[g - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 786291	NM_024706.5(ZNF668):c.1859G>A (p.Ter620=)	ZNF668	Single nucleotide variant (synonymous variant)	ZNF668-related disorder +1 more	GBenign/Likely benign
Select item 3033694	NM_024706.5(ZNF668):c.1590G>C (p.Leu530=)	ZNF668	Single nucleotide variant (synonymous variant)	ZNF668-related disorder	GLikely benign
Select item 3043623	NM_024706.5(ZNF668):c.1041G>A (p.Ala347=)	ZNF668	Single nucleotide variant (synonymous variant)	ZNF668-related disorder	GLikely benign
Select item 3030139	NM_024706.5(ZNF668):c.273G>A (p.Lys91=)	ZNF668	Single nucleotide variant (synonymous variant)	ZNF668-related disorder	GLikely benign
Select item 3042322	NM_024706.5(ZNF668):c.-22-107G>A	ZNF668 (D11N)	Single nucleotide variant (missense variant +1 more)	ZNF668-related disorder	GLikely benign

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