"Baylor Genetics"[submitter] AND "RNF213"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1033795	NM_001256071.3(RNF213):c.1837G>T (p.Asp613Tyr)	RNF213 (D613Y)	Single nucleotide variant (missense variant)	Moyamoya disease 2	GUncertain significance
Select item 1033794	NM_001256071.3(RNF213):c.13997C>T (p.Thr4666Ile)	RNF213, RNF213-AS1 (T4666I)	Single nucleotide variant (missense variant)	Moyamoya disease 2	GUncertain significance