"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC130066 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 338679	NM_006420.3(ARFGEF2):c.-43G>A	ARFGEF2, LOC130066080	Single nucleotide variant (5 prime UTR variant)	ARFGEF2-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 418016	NM_006420.3(ARFGEF2):c.-24_-1del	LOC130066080, ARFGEF2	Deletion (5 prime UTR variant)	not specified +1 more	GLikely benign