"Gharavi Laboratory, Columbia University"[submitter] AND "LOC109610631 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 589881	NM_139058.3(ARX):c.451_465del (p.Ala151_Ala155del)	ARX, LOC109610631	Deletion (inframe_deletion)	Inborn genetic diseases +3 more	GConflicting classifications of pathogenicity
Select item 591328	NM_139058.3(ARX):c.306GGC[5] (p.Ala111_Ala115del)	LOC109610631, ARX	Microsatellite (inframe_deletion)	Developmental and epileptic encephalopathy, 1 +2 more	GConflicting classifications of pathogenicity