ClinVar Miner

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

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_172201.2(KCNE2):c.79C>T (p.Arg27Cys)	rs74315449	0.00006
NM_172201.2(KCNE2):c.347C>T (p.Ala116Val)	rs199473367	0.00003

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