List of variants in gene combination LOC110121269, SCN5A reported as benign for long QT syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.3183A>G (p.Glu1061=)	rs7430407	0.90302
NM_000335.5(SCN5A):c.2788-6C>T	rs41260344	0.04241
NM_000335.5(SCN5A):c.3305C>A (p.Ser1102Tyr)	rs7626962	0.02208
NM_000335.5(SCN5A):c.3010T>C (p.Cys1004Arg)	rs199473183	0.00029

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