List of variants in gene SNTA1 reported as likely benign for Congenital 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.807T>C (p.Asn269=)	rs73270015	0.02196
NM_003098.3(SNTA1):c.*343G>A	rs41305789	0.02092
NM_003098.3(SNTA1):c.1350C>T (p.Phe450=)	rs116747979	0.01203
NM_003098.3(SNTA1):c.555C>T (p.Val185=)	rs34995247	0.00948
NM_003098.3(SNTA1):c.*342C>T	rs150740903	0.00900
NM_003098.3(SNTA1):c.497-7C>T	rs116972153	0.00063
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser)	rs150576530	0.00054
NM_003098.3(SNTA1):c.*122G>A	rs116151218

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