C1846689[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2444199	NM_001256071.3(RNF213):c.11999G>A (p.Cys4000Tyr)	RNF213, RNF213-AS1 (C4000Y +1 more)	Single nucleotide variant (missense variant)	Moyamoya disease 2	GUncertain significance
Select item 39700	NM_001256071.3(RNF213):c.14429G>A (p.Arg4810Lys)	RNF213, RNF213-AS1 (R4810K)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity