List of variants in gene KCNJ2 reported as benign for cardiac rhythm disease

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

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000891.3(KCNJ2):c.*1267A>G	rs236514	0.52229
NM_000891.3(KCNJ2):c.1146C>T (p.Leu382=)	rs173135	0.12771
NM_000891.3(KCNJ2):c.*1069C>T	rs45603434	0.09819
NM_000891.3(KCNJ2):c.*624G>A	rs9302915	0.07098
NM_000891.3(KCNJ2):c.*558C>T	rs9302914	0.06842
NM_000891.3(KCNJ2):c.*136G>A	rs73998781	0.06798
NM_000891.3(KCNJ2):c.660C>T (p.Ser220=)	rs7221086	0.06793
NM_000891.3(KCNJ2):c.*1198A>G	rs9895478	0.06787
NM_000891.3(KCNJ2):c.*1251C>T	rs9894661	0.06785
NM_000891.3(KCNJ2):c.*1266C>T	rs9894677	0.06783
NM_000891.3(KCNJ2):c.*832G>A	rs10083831	0.06743
NM_000891.3(KCNJ2):c.*2752T>C	rs993085233	0.04719
NM_000891.3(KCNJ2):c.*2758T>C	rs1324652195	0.04554
NM_000891.3(KCNJ2):c.*3496T>C	rs3815307	0.01760
NM_000891.3(KCNJ2):c.*1678dup	rs145779709
NM_000891.3(KCNJ2):c.*640GTT[4]	rs397705636

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