C0007787[trait identifier] AND "Centre for Mendelian Genomics, Univers - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 523370	NM_000435.3(NOTCH3):c.1450T>G (p.Cys484Gly)	NOTCH3 (C484G)	Single nucleotide variant (missense variant)	Migraine +3 more	GLikely pathogenic
Select item 208501	NM_000435.3(NOTCH3):c.457C>T (p.Arg153Cys)	NOTCH3 (R153C)	Single nucleotide variant (missense variant)	Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 +3 more	GPathogenic/Likely pathogenic