ClinVar Miner

List of variants in gene KCNJ10 reported as uncertain significance by GeneDx

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002241.5(KCNJ10):c.136G>A (p.Asp46Asn) rs141553756 0.00146
NM_002241.5(KCNJ10):c.530A>G (p.Glu177Gly) rs145947380 0.00043
NM_002241.5(KCNJ10):c.52C>T (p.Arg18Trp) rs138457635 0.00041
NM_002241.5(KCNJ10):c.1043G>A (p.Arg348His) rs146396982 0.00034
NM_002241.5(KCNJ10):c.1061A>G (p.Lys354Arg) rs142596580 0.00029
NM_002241.5(KCNJ10):c.148C>T (p.Leu50Phe) rs773510302 0.00019
NM_002241.5(KCNJ10):c.1102G>C (p.Glu368Gln) rs377330985 0.00013
NM_002241.5(KCNJ10):c.301C>A (p.Pro101Thr) rs375361490 0.00011
NM_002241.5(KCNJ10):c.1042C>T (p.Arg348Cys) rs137853074 0.00008
NM_002241.5(KCNJ10):c.1123C>T (p.Arg375Cys) rs751338154 0.00008
NM_002241.5(KCNJ10):c.401G>A (p.Arg134His) rs368857205 0.00005
NM_002241.5(KCNJ10):c.238T>G (p.Phe80Val) rs377638115 0.00003
NM_002241.5(KCNJ10):c.331C>G (p.Gln111Glu) rs1264459433 0.00002
NM_002241.5(KCNJ10):c.1027C>T (p.Arg343Cys) rs753333164 0.00001
NM_002241.5(KCNJ10):c.1051G>A (p.Asp351Asn) rs373899425 0.00001
NM_002241.5(KCNJ10):c.133G>A (p.Ala45Thr) rs750246232 0.00001
NM_002241.5(KCNJ10):c.142C>T (p.Arg48Cys) rs754056344 0.00001
NM_002241.5(KCNJ10):c.179T>C (p.Ile60Thr) rs759993423 0.00001
NM_002241.5(KCNJ10):c.250G>A (p.Val84Met) rs140646329 0.00001
NM_002241.5(KCNJ10):c.427G>A (p.Ala143Thr) rs796052607 0.00001
NM_002241.5(KCNJ10):c.652C>T (p.Leu218Phe) rs558502886 0.00001
NM_002241.5(KCNJ10):c.998T>C (p.Val333Ala) rs750091894 0.00001
NM_002241.5(KCNJ10):c.-1+1G>A rs796052606
NM_002241.5(KCNJ10):c.1006G>A (p.Val336Met) rs1085307763
NM_002241.5(KCNJ10):c.1006G>C (p.Val336Leu) rs1085307763
NM_002241.5(KCNJ10):c.1021G>C (p.Gly341Arg) rs796052605
NM_002241.5(KCNJ10):c.112A>G (p.Asn38Asp) rs1085307764
NM_002241.5(KCNJ10):c.124G>A (p.Glu42Lys) rs794727265
NM_002241.5(KCNJ10):c.296T>C (p.Leu99Pro) rs540341763
NM_002241.5(KCNJ10):c.300C>A (p.Asp100Glu) rs139069413
NM_002241.5(KCNJ10):c.539G>A (p.Arg180His) rs1131691880
NM_002241.5(KCNJ10):c.685A>G (p.Ile229Val) rs767156961
NM_002241.5(KCNJ10):c.685A>T (p.Ile229Phe) rs767156961
NM_002241.5(KCNJ10):c.955G>A (p.Ala319Thr)

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