List of variants in gene RBM20 reported as uncertain significance for long QT syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001134363.3(RBM20):c.776G>T (p.Gly259Val)	rs940901720	0.00001
NM_001134363.3(RBM20):c.2390A>T (p.His797Leu)
NM_001134363.3(RBM20):c.2715G>A (p.Met905Ile)

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