List of variants in gene KCNJ10 reported as likely benign for not provided

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.53G>A (p.Arg18Gln)	rs115466046	0.01096
NM_002241.5(KCNJ10):c.*2242T>C	rs115120891	0.00948
NM_002241.5(KCNJ10):c.*137G>A	rs115725914	0.00699
NM_002241.5(KCNJ10):c.*2596A>G	rs116418256	0.00551
NM_002241.5(KCNJ10):c.*2803T>G	rs148334590	0.00476
NM_002241.5(KCNJ10):c.*1161T>C	rs149832483	0.00464
NM_002241.5(KCNJ10):c.*2034C>T	rs192835895	0.00345
NM_002241.5(KCNJ10):c.1092A>G (p.Gln364=)	rs145588542	0.00339
NM_002241.5(KCNJ10):c.812G>A (p.Arg271His)	rs3795339	0.00113
NM_002241.5(KCNJ10):c.219G>A (p.Ala73=)	rs144495959	0.00016
NM_002241.5(KCNJ10):c.688C>T (p.Arg230Trp)	rs149615470	0.00014
NM_002241.5(KCNJ10):c.305C>T (p.Pro102Leu)	rs372156619	0.00010
NM_002241.5(KCNJ10):c.114C>T (p.Asn38=)	rs151068619	0.00008
NM_002241.5(KCNJ10):c.405C>T (p.Tyr135=)	rs765590257	0.00007
NM_002241.5(KCNJ10):c.39T>A (p.Thr13=)	rs776805483	0.00006
NM_002241.5(KCNJ10):c.240C>T (p.Phe80=)	rs774758209	0.00005
NM_002241.5(KCNJ10):c.1137C>G (p.Val379=)	rs372774976	0.00004
NM_002241.5(KCNJ10):c.135C>T (p.Ala45=)	rs1397547909	0.00004
NM_002241.5(KCNJ10):c.705T>C (p.Asn235=)	rs554749579	0.00004
NM_002241.5(KCNJ10):c.729C>T (p.Ala243=)	rs756703582	0.00002
NM_002241.5(KCNJ10):c.21G>A (p.Val7=)	rs750227861	0.00001
NM_002241.5(KCNJ10):c.300C>A (p.Asp100Glu)	rs139069413
NM_002241.5(KCNJ10):c.459C>T (p.Leu153=)	rs1467302352

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