ClinVar Miner

List of variants in gene KCNJ2 reported as uncertain significance for not provided

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000891.3(KCNJ2):c.1229A>G (p.Asn410Ser) rs141069645 0.00042
NM_000891.3(KCNJ2):c.1045G>A (p.Glu349Lys) rs375330016 0.00015
NM_000891.3(KCNJ2):c.1244C>T (p.Pro415Leu) rs373799322 0.00013
NM_000891.3(KCNJ2):c.168T>C (p.Val56=) rs370111593 0.00011
NM_000891.3(KCNJ2):c.616G>A (p.Gly206Ser) rs141035459 0.00011
NM_000891.3(KCNJ2):c.277G>A (p.Val93Ile) rs147750704 0.00007
NM_000891.3(KCNJ2):c.973C>T (p.Arg325Cys) rs202067116 0.00007
NM_000891.3(KCNJ2):c.208G>T (p.Ala70Ser) rs375605948 0.00005
NM_000891.3(KCNJ2):c.1199C>T (p.Thr400Met) rs144022753 0.00004
NM_000891.3(KCNJ2):c.119G>A (p.Arg40Gln) rs766143485 0.00004
NM_000891.3(KCNJ2):c.511A>G (p.Ile171Val) rs150326473 0.00004
NM_000891.3(KCNJ2):c.359A>C (p.Lys120Thr) rs375646186 0.00003
NM_000891.3(KCNJ2):c.1165G>A (p.Asp389Asn) rs140053197 0.00002
NM_000891.3(KCNJ2):c.236T>C (p.Ile79Thr) rs786205813 0.00002
NM_000891.3(KCNJ2):c.166G>A (p.Val56Ile) rs1264595509 0.00001
NM_000891.3(KCNJ2):c.179A>G (p.Asn60Ser) rs1484750176 0.00001
NM_000891.3(KCNJ2):c.261C>T (p.Ile87=) rs1166497262 0.00001
NM_000891.3(KCNJ2):c.302G>T (p.Cys101Phe) rs750630010 0.00001
NM_000891.3(KCNJ2):c.389C>T (p.Thr130Met) rs151168735 0.00001
NM_000891.3(KCNJ2):c.637C>T (p.Arg213Ter) rs764523123 0.00001
NM_000891.3(KCNJ2):c.752A>G (p.Asn251Ser) rs1261477163 0.00001
NM_000891.3(KCNJ2):c.781A>G (p.Ile261Val) rs774461588 0.00001
NM_000891.3(KCNJ2):c.845T>G (p.Leu282Trp) rs758092571 0.00001
NM_000891.3(KCNJ2):c.953A>G (p.Asn318Ser) rs367560052 0.00001
NM_000891.3(KCNJ2):c.974G>A (p.Arg325His) rs1555604000 0.00001
NM_000891.3(KCNJ2):c.1006TAC[1] (p.Tyr337del) rs1555604002
NM_000891.3(KCNJ2):c.1091A>G (p.Lys364Arg) rs1060500054
NM_000891.3(KCNJ2):c.1106C>T (p.Ser369Leu) rs2144377947
NM_000891.3(KCNJ2):c.118C>T (p.Arg40Ter) rs786205811
NM_000891.3(KCNJ2):c.1217T>C (p.Ile406Thr) rs202149686
NM_000891.3(KCNJ2):c.1267C>T (p.Arg423Ter) rs2074392920
NM_000891.3(KCNJ2):c.1274C>T (p.Ser425Leu)
NM_000891.3(KCNJ2):c.137G>A (p.Arg46His)
NM_000891.3(KCNJ2):c.169C>T (p.Gln57Ter)
NM_000891.3(KCNJ2):c.17C>T (p.Thr6Ile) rs754091630
NM_000891.3(KCNJ2):c.251T>C (p.Met84Thr)
NM_000891.3(KCNJ2):c.256G>A (p.Val86Ile)
NM_000891.3(KCNJ2):c.256G>T (p.Val86Phe) rs786205814
NM_000891.3(KCNJ2):c.278T>C (p.Val93Ala) rs1025972346
NM_000891.3(KCNJ2):c.289C>A (p.Leu97Met) rs2144376749
NM_000891.3(KCNJ2):c.2T>C (p.Met1Thr) rs786205810
NM_000891.3(KCNJ2):c.328C>T (p.His110Tyr) rs786205815
NM_000891.3(KCNJ2):c.346T>C (p.Ser116Pro) rs2144376847
NM_000891.3(KCNJ2):c.394_396dup (p.Ala132dup) rs786205821
NM_000891.3(KCNJ2):c.416C>T (p.Thr139Ile) rs1060500052
NM_000891.3(KCNJ2):c.436G>C (p.Gly146Arg) rs199473654
NM_000891.3(KCNJ2):c.529G>A (p.Gly177Ser) rs1555603949
NM_000891.3(KCNJ2):c.578T>C (p.Leu193Pro) rs1555603955
NM_000891.3(KCNJ2):c.608T>C (p.Met203Thr)
NM_000891.3(KCNJ2):c.659G>A (p.Ser220Asn) rs2074388522
NM_000891.3(KCNJ2):c.778C>T (p.Arg260Cys) rs2144377429
NM_000891.3(KCNJ2):c.794C>G (p.Ser265Cys) rs1598211406
NM_000891.3(KCNJ2):c.806T>A (p.Ile269Lys) rs886042211
NM_000891.3(KCNJ2):c.821A>T (p.Asp274Val) rs786205816
NM_000891.3(KCNJ2):c.853C>T (p.Gln285Ter) rs776976697
NM_000891.3(KCNJ2):c.884T>C (p.Val295Ala) rs201162707
NM_000891.3(KCNJ2):c.887T>C (p.Val296Ala)
NM_000891.3(KCNJ2):c.907G>C (p.Glu303Gln) rs199473386
NM_000891.3(KCNJ2):c.941C>T (p.Ser314Phe) rs1598211503
NM_000891.3(KCNJ2):c.976T>A (p.Tyr326Asn) rs786205819
NM_000891.3(KCNJ2):c.97G>A (p.Gly33Arg) rs375727662

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