C2678478[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 856436	NM_000719.7(CACNA1C):c.200G>A (p.Ser67Asn)	CACNA1C (S67N)	Single nucleotide variant (missense variant)	Long QT syndrome +1 more	GUncertain significance
Select item 1030883	NM_000719.7(CACNA1C):c.694G>C (p.Asp232His)	CACNA1C (D232H)	Single nucleotide variant (missense variant)	CACNA1C-related disorder +1 more	GUncertain significance
Select item 17632	NM_000719.7(CACNA1C):c.1216G>A (p.Gly406Arg)	CACNA1C (G406R +1 more)	Single nucleotide variant (missense variant +1 more)	Long QT syndrome +7 more	GPathogenic

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