List of variants in gene KCNJ5 reported as likely pathogenic 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
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_000890.5(KCNJ5):c.1159G>C (p.Gly387Arg)	rs199830292	0.00008
NM_000890.5(KCNJ5):c.473C>G (p.Thr158Arg)	rs145901904	0.00001

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