List of variants in gene SCN4B reported as uncertain significance for Long QT syndrome

Minimum submission review status:		Collection method:
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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_174934.4(SCN4B):c.607G>A (p.Val203Met)	rs150312046	0.00031
NM_174934.4(SCN4B):c.*1343C>T	rs886047723	0.00001
NM_174934.4(SCN4B):c.*434T>C	rs886047729	0.00001
NM_174934.4(SCN4B):c.*1993del	rs886047721
NM_174934.4(SCN4B):c.*3632del	rs886047715
NM_174934.4(SCN4B):c.*989dup	rs5795117
NM_174934.4(SCN4B):c.*990del	rs747111771

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