List of variants in gene CTNNA3 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_013266.4(CTNNA3):c.377G>A (p.Arg126His)	rs730880071	0.00005
NM_013266.4(CTNNA3):c.35A>T (p.Asp12Val)	rs730880069	0.00004

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