C4551804[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 532063	NM_000335.5(SCN5A):c.6004G>A (p.Asp2002Asn)	SCN5A (D2002N +5 more)	Single nucleotide variant (missense variant)	not specified +11 more	GUncertain significance
Select item 201589	NM_000335.5(SCN5A):c.4168G>A (p.Gly1390Arg)	SCN5A (G1390R +2 more)	Single nucleotide variant (missense variant)	not provided +10 more	GUncertain significance
Select item 67835	NM_000335.5(SCN5A):c.3908C>T (p.Thr1303Met)	SCN5A (T1303M +2 more)	Single nucleotide variant (missense variant)	Conduction disorder of the heart +6 more	GUncertain significance
Select item 2582527	NM_000335.5(SCN5A):c.2677C>A (p.Arg893Ser)	SCN5A (R893S)	Single nucleotide variant (missense variant +1 more)	Brugada syndrome 1	GLikely pathogenic
Select item 201559	NM_000335.5(SCN5A):c.2533del (p.Val845fs)	SCN5A (V845fs)	Deletion (frameshift variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 67712	NM_000335.5(SCN5A):c.2074C>A (p.Gln692Lys)	SCN5A (Q692K)	Single nucleotide variant (missense variant)	Long QT syndrome +11 more	GConflicting classifications of pathogenicity
Select item 67678	NM_000335.5(SCN5A):c.1700T>A (p.Leu567Gln)	SCN5A (L567Q)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 10 +5 more	GUncertain significance
Select item 67657	NM_000335.5(SCN5A):c.1340C>G (p.Ala447Gly)	SCN5A (A447G)	Single nucleotide variant (missense variant)	not specified +11 more	GConflicting classifications of pathogenicity

ClinVar