List of variants in gene SNTA1 reported as uncertain significance 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.828G>A (p.Lys276=)	rs35938843	0.00969
NM_003098.3(SNTA1):c.993C>T (p.Arg331=)	rs143309917	0.00125
NM_003098.3(SNTA1):c.984C>T (p.Pro328=)	rs138863915	0.00121
NM_003098.3(SNTA1):c.787G>T (p.Ala263Ser)	rs150576530	0.00054
NM_003098.3(SNTA1):c.*79C>A	rs78892511	0.00040
NM_003098.3(SNTA1):c.1118G>A (p.Arg373His)	rs754648214	0.00002
NM_003098.3(SNTA1):c.1205G>A (p.Arg402Gln)	rs771369802	0.00002
NM_003098.3(SNTA1):c.1479C>T (p.Phe493=)	rs559827815	0.00002
NM_003098.3(SNTA1):c.*6G>A	rs565582070	0.00001
NM_003098.3(SNTA1):c.1181G>A (p.Arg394His)	rs750278583	0.00001
NM_003098.3(SNTA1):c.1256G>A (p.Arg419His)	rs751302839	0.00001
NM_003098.3(SNTA1):c.514G>A (p.Val172Ile)	rs775580363	0.00001
NM_003098.3(SNTA1):c.1238-13G>C	rs748801869
NM_003098.3(SNTA1):c.651G>A (p.Leu217=)	rs886056626

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