"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC108644 - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042006	NM_003418.5(CNBP):c.-14-837_-14-830del	CNBP, LOC108644431	Microsatellite (intron variant)	CNBP-related disorder	GLikely benign
Select item 3043208	NM_003418.5(CNBP):c.-14-857_-14-838del	CNBP, LOC108644431	Deletion (intron variant)	CNBP-related disorder	GLikely benign
Select item 3033016	NM_003418.5(CNBP):c.-14-853_-14-838del	CNBP, LOC108644431	Deletion (intron variant)	CNBP-related disorder	GLikely benign
Select item 3030761	NM_003418.5(CNBP):c.-14-962GT[18]	CNBP, LOC108644431	Microsatellite (intron variant)	CNBP-related disorder	GLikely benign

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