List of variants in gene combination KCNE2, LOC105372791 reported as benign for long QT syndrome 6

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_172201.2(KCNE2):c.-79G>A	rs41260744	0.07525
NM_172201.2(KCNE2):c.-52G>A	rs41314699	0.00570
NM_172201.2(KCNE2):c.25C>G (p.Gln9Glu)	rs16991652	0.00468
NM_172201.2(KCNE2):c.22A>G (p.Thr8Ala)	rs2234916	0.00387
NM_172201.2(KCNE2):c.354G>A (p.Gly118=)	rs187917779	0.00019

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