List of variants in gene combination LOC110121269, SCN5A reported as likely pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.3157G>A (p.Glu1053Lys)	rs137854617	0.00016
NM_000335.5(SCN5A):c.2989G>T (p.Ala997Ser)	rs137854609
NM_000335.5(SCN5A):c.3273del (p.Arg1092fs)

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