C4012050[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1031118	NM_133459.4(CCBE1):c.901C>T (p.Arg301Trp)	CCBE1 (R301W)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1031117	NM_133459.4(CCBE1):c.845G>A (p.Arg282Gln)	CCBE1 (R282Q)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1031116	NM_133459.4(CCBE1):c.274G>A (p.Val92Ile)	CCBE1 (V92I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

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