ClinVar Miner

List of variants in gene KCNJ10 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002241.5(KCNJ10):c.*2040C>G rs2486254 0.99734
NM_002241.5(KCNJ10):c.*2062T>G rs1053074 0.45911
NM_002241.5(KCNJ10):c.1-171C>T rs3120973 0.23525
NM_002241.5(KCNJ10):c.-1+153C>T rs2820585 0.21737
NM_002241.5(KCNJ10):c.1-84T>C rs12729701 0.18530
NM_002241.5(KCNJ10):c.811C>T (p.Arg271Cys) rs1130183 0.04770
NM_002241.5(KCNJ10):c.*413G>A rs79238495 0.02238
NM_002241.5(KCNJ10):c.53G>A (p.Arg18Gln) rs115466046 0.01096
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.615A>G (p.Lys205=) rs142228240 0.00066
NM_002241.5(KCNJ10):c.219G>A (p.Ala73=) rs144495959 0.00016
NM_002241.5(KCNJ10):c.-44del rs1018660154 0.00009
NM_002241.5(KCNJ10):c.-43G>A rs372841245 0.00004
NM_002241.5(KCNJ10):c.927C>T (p.Tyr309=) rs775091787 0.00002
NM_002241.5(KCNJ10):c.*1764T>G rs2486253
NM_002241.5(KCNJ10):c.*1813C>A rs78280261
NM_002241.5(KCNJ10):c.*1970GT[18] rs56656397
NM_002241.5(KCNJ10):c.*1970GT[21] rs56656397
NM_002241.5(KCNJ10):c.*1970GT[22] rs56656397
NM_002241.5(KCNJ10):c.*1970GT[23] rs56656397
NM_002241.5(KCNJ10):c.*1970GT[24] rs56656397
NM_002241.5(KCNJ10):c.*1970GT[26] rs56656397
NM_002241.5(KCNJ10):c.234A>C (p.Thr78=) rs748359138

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.