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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033241	NM_001164803.2(RBMX):c.559_561del (p.Tyr187del)	RBMX (Y187del)	Deletion (inframe_deletion)	RBMX-related disorder	GBenign
Select item 3030440	NM_002139.4(RBMX):c.931GAT[1] (p.Asp312del)	LOC126863330, RBMX (D312del)	Microsatellite (inframe deletion +2 more)	RBMX-related disorder	GUncertain significance
Select item 2637364	NM_002139.4(RBMX):c.101T>A (p.Ile34Lys)	RBMX (I34K)	Single nucleotide variant (missense variant +1 more)	RBMX-related disorder	GUncertain significance

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