List of variants in gene SNTA1 reported as likely pathogenic 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_003098.3(SNTA1):c.1169C>T (p.Ala390Val)	rs121434500	0.00001
NM_003098.3(SNTA1):c.1498C>T (p.Arg500Cys)	rs786205426

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