List of variants in gene KCNJ5 reported as likely benign by Illumina Laboratory Services, Illumina

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_000890.5(KCNJ5):c.*34G>T	rs116494206	0.01052
NM_000890.5(KCNJ5):c.*449A>T	rs115414355	0.00584
NM_000890.5(KCNJ5):c.*759C>T	rs75453162	0.00373
NM_000890.5(KCNJ5):c.*547G>A	rs114896724	0.00370
NM_000890.5(KCNJ5):c.121C>T (p.Arg41Cys)	rs115012103	0.00300
NM_000890.5(KCNJ5):c.*1216C>T	rs566376081	0.00293
NM_000890.5(KCNJ5):c.*1091G>A	rs565178107	0.00218
NM_000890.5(KCNJ5):c.*96G>A	rs77092337	0.00200
NM_000890.5(KCNJ5):c.*1302C>T	rs552826605	0.00089
NM_000890.5(KCNJ5):c.*977T>C	rs181648220	0.00068
NM_000890.5(KCNJ5):c.957G>A (p.Arg319=)	rs192889782	0.00051
NM_000890.5(KCNJ5):c.-63G>C	rs557063967	0.00044
NM_000890.5(KCNJ5):c.273C>T (p.Leu91=)	rs146853795	0.00037
NM_000890.5(KCNJ5):c.744G>A (p.Glu248=)	rs144040058	0.00037
NM_000890.5(KCNJ5):c.*1310C>T	rs537850039	0.00033
NM_000890.5(KCNJ5):c.*960G>C	rs186315097	0.00022
NM_000890.5(KCNJ5):c.1159G>C (p.Gly387Arg)	rs199830292	0.00008
NM_000890.5(KCNJ5):c.1254G>A (p.Ser418=)	rs528463709	0.00005
NM_000890.5(KCNJ5):c.430A>G (p.Ile144Val)	rs369703183	0.00002
NM_000890.5(KCNJ5):c.*121G>T	rs78979538
NM_000890.5(KCNJ5):c.*936C>T	rs77525858

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