List of variants in gene combination LOC130065679, 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.255G>C (p.Arg85=)	rs1335742203	0.00003
NM_003098.3(SNTA1):c.279C>A (p.Ala93=)	rs1178951223
NM_003098.3(SNTA1):c.292C>T (p.Leu98=)	rs2146814454

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