List of variants in gene combination LOC130065679, SNTA1 reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.287G>C (p.Gly96Ala)	rs766925398	0.00014
NM_003098.3(SNTA1):c.272G>T (p.Arg91Leu)
NM_003098.3(SNTA1):c.273dup (p.Lys92fs)
NM_003098.3(SNTA1):c.275A>G (p.Lys92Arg)
NM_003098.3(SNTA1):c.277G>A (p.Ala93Thr)	rs886056627
NM_003098.3(SNTA1):c.280G>C (p.Asp94His)	rs786205844
NM_003098.3(SNTA1):c.304dup (p.Ile102fs)

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