C1846171[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1526057	NM_139058.3(ARX):c.1206del (p.Pro403fs)	ARX (P403fs)	Deletion (frameshift variant)	X-linked lissencephaly with abnormal genitalia	GLikely pathogenic
Select item 11186	NM_139058.3(ARX):c.306GGC[17] (p.Ala109_Ala115dup)	ARX, LOC109610631	Microsatellite (inframe_insertion)	Inborn genetic diseases +5 more	GPathogenic/Likely pathogenic