C1864041[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1030944	NM_031443.4(CCM2):c.643C>T (p.Gln215Ter)	CCM2 (Q157* +2 more)	Single nucleotide variant (nonsense +2 more)	Cerebral cavernous malformation 2	GPathogenic
Select item 1034110	NM_031443.4(CCM2):c.830G>A (p.Gly277Asp)	CCM2 (G260D +5 more)	Single nucleotide variant (missense variant +1 more)	Cerebral cavernous malformation 2	GUncertain significance