List of variants in gene combination LOC130065680, 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003098.3(SNTA1):c.128G>A (p.Ser43Asn)	rs786205841	0.00022
NM_003098.2(SNTA1):c.-200C>T	rs879769686	0.00012
NM_003098.3(SNTA1):c.-261C>A	rs536994978	0.00010
NM_003098.3(SNTA1):c.-262C>T	rs550104436	0.00010
NM_003098.2(SNTA1):c.-251G>A	rs886056630	0.00001
NM_003098.3(SNTA1):c.-18G>A	rs886056628	0.00001
NM_003098.2(SNTA1):c.-186C>T	rs886056629
NM_003098.3(SNTA1):c.-96G>C	rs145471317

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