List of variants in gene LOC130006838, SCN4B studied for long QT syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_174934.4(SCN4B):c.62-13G>A	rs747651845	0.00003
NM_174934.4(SCN4B):c.62-16G>A	rs772762943	0.00001
NM_174934.4(SCN4B):c.62-1G>A	rs950065814	0.00001
NM_174934.4(SCN4B):c.62-15G>C
NM_174934.4(SCN4B):c.62-19G>T
NM_174934.4(SCN4B):c.62-5C>T	rs2135505353
NM_174934.4(SCN4B):c.62-7T>C

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