List of variants in gene KCNJ5 reported as likely benign by GeneDx

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: 32

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000890.5(KCNJ5):c.*34G>T	rs116494206	0.01052
NM_000890.5(KCNJ5):c.*759C>T	rs75453162	0.00373
NM_000890.5(KCNJ5):c.-10-81C>T	rs558263934	0.00322
NM_000890.5(KCNJ5):c.*1091G>A	rs565178107	0.00218
NM_000890.5(KCNJ5):c.192C>T (p.His64=)	rs140848236	0.00182
NM_000890.5(KCNJ5):c.837G>A (p.Glu279=)	rs149861510	0.00087
NM_000890.5(KCNJ5):c.1149C>T (p.Pro383=)	rs143219149	0.00078
NM_000890.5(KCNJ5):c.744G>A (p.Glu248=)	rs144040058	0.00037
NM_000890.5(KCNJ5):c.825C>A (p.Ile275=)	rs113012271	0.00034
NM_000890.5(KCNJ5):c.1158G>C (p.Leu386=)	rs141325005	0.00026
NM_000890.5(KCNJ5):c.122G>A (p.Arg41His)	rs139073333	0.00025
NM_000890.5(KCNJ5):c.630G>A (p.Met210Ile)	rs138295501	0.00016
NM_000890.5(KCNJ5):c.133G>A (p.Glu45Lys)	rs372447456	0.00011
NM_000890.5(KCNJ5):c.1152A>G (p.Pro384=)	rs987098040	0.00010
NM_000890.5(KCNJ5):c.312C>T (p.Phe104=)	rs201217363	0.00009
NM_000890.5(KCNJ5):c.792C>T (p.Gly264=)	rs750600982	0.00009
NM_000890.5(KCNJ5):c.738G>A (p.Glu246=)	rs372736753	0.00008
NM_000890.5(KCNJ5):c.366C>T (p.Gly122=)	rs375205252	0.00004
NM_000890.5(KCNJ5):c.795C>T (p.Asp265=)	rs757895735	0.00003
NM_000890.5(KCNJ5):c.1032T>C (p.Tyr344=)	rs185384497	0.00002
NM_000890.5(KCNJ5):c.723C>A (p.Ser241=)	rs757420915	0.00002
NM_000890.5(KCNJ5):c.-11+14T>C	rs1436945797	0.00001
NM_000890.5(KCNJ5):c.90C>T (p.Arg30=)	rs201886526	0.00001
NM_000890.5(KCNJ5):c.990C>A (p.Gly330=)	rs1370256653	0.00001
NM_000890.5(KCNJ5):c.*861GTTTT[6]	rs36205004
NM_000890.5(KCNJ5):c.*936C>T	rs77525858
NM_000890.5(KCNJ5):c.-293GA[3]	rs886047996
NM_000890.5(KCNJ5):c.-293GA[4]	rs886047996
NM_000890.5(KCNJ5):c.-293GA[5]	rs886047996
NM_000890.5(KCNJ5):c.750C>T (p.Ile250=)	rs1305792469
NM_000890.5(KCNJ5):c.938-164GATG[14]	rs61176061
NM_000890.5(KCNJ5):c.938-210TGGA[7]	rs201935642

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.