List of variants in gene combination KCNE3, LIPT2 reported as uncertain significance for heart conduction disease

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005472.5(KCNE3):c.248G>A (p.Arg83His)	rs17215437	0.00338
NM_005472.5(KCNE3):c.10A>G (p.Thr4Ala)	rs200856070	0.00002

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