"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "RN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 284163	NM_152617.4(RNF168):c.1237G>A (p.Glu413Lys)	RNF168 (E413K)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign
Select item 403381	NM_152617.4(RNF168):c.1202C>A (p.Pro401Gln)	RNF168 (P401Q)	Single nucleotide variant (missense variant)	RIDDLE syndrome +2 more	GBenign
Select item 218846	NM_152617.4(RNF168):c.508G>A (p.Glu170Lys)	RNF168 (E170K)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign

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