List of variants in gene KCNJ10 reported as likely benign by Ambry Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_002241.5(KCNJ10):c.1092A>G (p.Gln364=)	rs145588542	0.00339
NM_002241.5(KCNJ10):c.735C>G (p.Asp245Glu)	rs146426296	0.00155
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.114C>T (p.Asn38=)	rs151068619	0.00008
NM_002241.5(KCNJ10):c.1047C>T (p.Tyr349=)	rs368537434	0.00006
NM_002241.5(KCNJ10):c.225T>C (p.Phe75=)	rs757159382	0.00006
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.705T>C (p.Asn235=)	rs554749579	0.00004
NM_002241.5(KCNJ10):c.528T>C (p.Ala176=)	rs1057520295	0.00002
NM_002241.5(KCNJ10):c.234A>C (p.Thr78=)	rs748359138
NM_002241.5(KCNJ10):c.558T>G (p.Val186=)
NM_002241.5(KCNJ10):c.621C>T (p.Leu207=)
NM_002241.5(KCNJ10):c.684C>T (p.Asn228=)	rs533587041

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