C4551647[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9377	NM_000335.5(SCN5A):c.5347G>A (p.Glu1783Lys)	SCN5A (E1784K +5 more)	Single nucleotide variant (missense variant)	not provided +7 more	GPathogenic/Likely pathogenic
Select item 978356	NM_000238.4(KCNH2):c.1595T>C (p.Leu532Pro)	KCNH2 (L192P +4 more)	Single nucleotide variant (missense variant)	Long QT syndrome 2 +1 more	GConflicting classifications of pathogenicity
Select item 67399	NM_000238.4(KCNH2):c.243G>C (p.Gln81His)	KCNH2 (Q81H +1 more)	Single nucleotide variant (missense variant)	Long QT syndrome +2 more	GUncertain significance
Select item 53061	NM_000218.3(KCNQ1):c.532G>A (p.Ala178Thr)	KCNQ1 (A178T +2 more)	Single nucleotide variant (missense variant)	Cardiac arrhythmia +5 more	GPathogenic/Likely pathogenic
Select item 52936	NM_000218.3(KCNQ1):c.1031C>T (p.Ala344Val)	KCNQ1 (A344V +3 more)	Single nucleotide variant (missense variant)	Cardiac arrhythmia +4 more	GPathogenic
Select item 519296	NM_000218.3(KCNQ1):c.1520G>A (p.Arg507Gln)	KCNQ1 (R380Q +4 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1 +7 more	GUncertain significance
Select item 812678	NM_005184.4(CALM3):c.421G>A (p.Glu141Lys)	CALM3 (E141K +1 more)	Single nucleotide variant (missense variant)	Long QT syndrome 16 +1 more	GPathogenic

ClinVar