List of variants in gene combination LOC130065680, SNTA1 reported as likely benign for 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003098.2(SNTA1):c.-255G>C	rs57684257	0.08518
NM_003098.3(SNTA1):c.-96G>A	rs145471317	0.01822
NM_003098.2(SNTA1):c.-245C>A	rs531929083	0.00728
NM_003098.3(SNTA1):c.36G>C (p.Leu12=)	rs949722422	0.00009
NM_003098.3(SNTA1):c.129C>T (p.Ser43=)	rs956270311	0.00008
NM_003098.3(SNTA1):c.13A>C (p.Arg5=)	rs980437334	0.00005
NM_003098.3(SNTA1):c.114C>T (p.Asp38=)	rs780018849	0.00003
NM_003098.3(SNTA1):c.123C>T (p.Thr41=)	rs1476277698
NM_003098.3(SNTA1):c.34C>T (p.Leu12=)	rs2146815323
NM_003098.3(SNTA1):c.42G>A (p.Glu14=)
NM_003098.3(SNTA1):c.51C>T (p.Ala17=)	rs1221002090
NM_003098.3(SNTA1):c.57G>T (p.Ala19=)	rs1288013630
NM_003098.3(SNTA1):c.75C>T (p.Gly25=)

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