C1859062[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

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	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 870402	NM_000335.5(SCN5A):c.3803A>G (p.Asn1268Ser)	SCN5A (N1215S +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GUncertain significance
Select item 67651	NM_000335.5(SCN5A):c.1231G>A (p.Val411Met)	SCN5A (V411M)	Single nucleotide variant (missense variant)	Long QT syndrome +3 more	GPathogenic

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