ClinVar Miner

List of variants in gene KCNJ2 studied for atrial fibrillation (disease)

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NM_000891.2(KCNJ2):c.*1069C>T rs45603434
NM_000891.2(KCNJ2):c.*1125G>A rs191729421
NM_000891.2(KCNJ2):c.*1128dup rs777658732
NM_000891.2(KCNJ2):c.*1198A>G rs9895478
NM_000891.2(KCNJ2):c.*122G>A rs886053324
NM_000891.2(KCNJ2):c.*124G>A rs886053325
NM_000891.2(KCNJ2):c.*1251C>T rs9894661
NM_000891.2(KCNJ2):c.*1267A>G rs236514
NM_000891.2(KCNJ2):c.*1350G>A rs116077770
NM_000891.2(KCNJ2):c.*1367T>C rs565257870
NM_000891.2(KCNJ2):c.*136G>A rs73998781
NM_000891.2(KCNJ2):c.*1412G>A rs886053331
NM_000891.2(KCNJ2):c.*1440A>T rs886053332
NM_000891.2(KCNJ2):c.*1596A>C rs117409545
NM_000891.2(KCNJ2):c.*1631C>G rs886053333
NM_000891.2(KCNJ2):c.*1678dup rs145779709
NM_000891.2(KCNJ2):c.*1702_*1703CT[3] rs1555604187
NM_000891.2(KCNJ2):c.*1702_*1704dup rs1555604193
NM_000891.2(KCNJ2):c.*1702dup rs886053334
NM_000891.2(KCNJ2):c.*1719_*1721dup rs35753731
NM_000891.2(KCNJ2):c.*1720_*1721dup rs35753731
NM_000891.2(KCNJ2):c.*1721dup rs35753731
NM_000891.2(KCNJ2):c.*1794C>A rs55864879
NM_000891.2(KCNJ2):c.*1815G>A rs552577704
NM_000891.2(KCNJ2):c.*2001A>G rs886053336
NM_000891.2(KCNJ2):c.*211T>C rs56194813
NM_000891.2(KCNJ2):c.*213G>A rs886053326
NM_000891.2(KCNJ2):c.*2262C>T rs575383136
NM_000891.2(KCNJ2):c.*2270G>T rs545863243
NM_000891.2(KCNJ2):c.*2277C>T rs185701493
NM_000891.2(KCNJ2):c.*2483G>A rs559751598
NM_000891.2(KCNJ2):c.*2526A>G rs886053337
NM_000891.2(KCNJ2):c.*2616A>G rs542407766
NM_000891.2(KCNJ2):c.*2663T>C rs886053338
NM_000891.2(KCNJ2):c.*2698T>C rs368668294
NM_000891.2(KCNJ2):c.*2754T>C rs9915769
NM_000891.2(KCNJ2):c.*2770_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2771_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2772_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2774_*2775del rs35656864
NM_000891.2(KCNJ2):c.*2775dup rs35656864
NM_000891.2(KCNJ2):c.*2776del rs886053343
NM_000891.2(KCNJ2):c.*2812T>C rs886053344
NM_000891.2(KCNJ2):c.*2875_*2876del rs561353262
NM_000891.2(KCNJ2):c.*2893C>T rs137870461
NM_000891.2(KCNJ2):c.*3025G>A rs536788614
NM_000891.2(KCNJ2):c.*3163T>A rs149224363
NM_000891.2(KCNJ2):c.*3208A>G rs188533495
NM_000891.2(KCNJ2):c.*324del rs570173316
NM_000891.2(KCNJ2):c.*3352T>A rs886053345
NM_000891.2(KCNJ2):c.*3353C>T rs886053346
NM_000891.2(KCNJ2):c.*3391_*3392dup rs552636156
NM_000891.2(KCNJ2):c.*3463del rs3841509
NM_000891.2(KCNJ2):c.*3496T>C rs3815307
NM_000891.2(KCNJ2):c.*3536C>T rs529969829
NM_000891.2(KCNJ2):c.*3618A>G rs530574251
NM_000891.2(KCNJ2):c.*558C>T rs9302914
NM_000891.2(KCNJ2):c.*596T>A rs886053328
NM_000891.2(KCNJ2):c.*624G>A rs9302915
NM_000891.2(KCNJ2):c.*640_*642GTT[4] rs397705636
NM_000891.2(KCNJ2):c.*687A>C rs886053329
NM_000891.2(KCNJ2):c.*732T>G rs150985434
NM_000891.2(KCNJ2):c.*766C>T rs186842823
NM_000891.2(KCNJ2):c.*79C>T rs55970278
NM_000891.2(KCNJ2):c.*832G>A rs10083831
NM_000891.2(KCNJ2):c.*996C>T rs77958248
NM_000891.2(KCNJ2):c.-162delinsTCAGAGTAGT rs376713253
NM_000891.2(KCNJ2):c.-195C>G rs544342049
NM_000891.2(KCNJ2):c.-228C>T rs765064661
NM_000891.2(KCNJ2):c.-258C>T rs886053321
NM_000891.2(KCNJ2):c.-2C>T rs144760658
NM_000891.2(KCNJ2):c.-314T>C rs566186294
NM_000891.2(KCNJ2):c.-349C>A rs370696463
NM_000891.2(KCNJ2):c.-88C>T rs886053322
NM_000891.2(KCNJ2):c.1146C>T (p.Leu382=) rs173135
NM_000891.2(KCNJ2):c.119G>A (p.Arg40Gln) rs766143485
NM_000891.2(KCNJ2):c.1229A>G (p.Asn410Ser) rs141069645
NM_000891.2(KCNJ2):c.1259C>T (p.Pro420Leu) rs749707062
NM_000891.2(KCNJ2):c.199C>T (p.Arg67Trp) rs104894580
NM_000891.2(KCNJ2):c.277G>A (p.Val93Ile) rs147750704
NM_000891.2(KCNJ2):c.344C>T (p.Ala115Val) rs886053323
NM_000891.2(KCNJ2):c.531C>T (p.Gly177=) rs544384907
NM_000891.2(KCNJ2):c.660C>T (p.Ser220=) rs7221086
NM_000891.3(KCNJ2):c.896A>G (p.Glu299Gly)

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