List of variants in gene KCNJ2 reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.1229A>G (p.Asn410Ser)	rs141069645	0.00038
NM_000891.3(KCNJ2):c.1002G>A (p.Lys334=)	rs372264881	0.00003
NM_000891.3(KCNJ2):c.117C>A (p.Thr39=)

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