ClinVar Miner

List of variants in gene KCNJ2 reported as likely benign for atrial fibrillation (disease)

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
NM_000891.2(KCNJ2):c.*1125G>A rs191729421
NM_000891.2(KCNJ2):c.*1350G>A rs116077770
NM_000891.2(KCNJ2):c.*1367T>C rs565257870
NM_000891.2(KCNJ2):c.*1596A>C rs117409545
NM_000891.2(KCNJ2):c.*1794C>A rs55864879
NM_000891.2(KCNJ2):c.*1815G>A rs552577704
NM_000891.2(KCNJ2):c.*2262C>T rs575383136
NM_000891.2(KCNJ2):c.*2277C>T rs185701493
NM_000891.2(KCNJ2):c.*2483G>A rs559751598
NM_000891.2(KCNJ2):c.*2616A>G rs542407766
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.*3496T>C rs3815307
NM_000891.2(KCNJ2):c.*3536C>T rs529969829
NM_000891.2(KCNJ2):c.*3618A>G rs530574251
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.*996C>T rs77958248
NM_000891.2(KCNJ2):c.-195C>G rs544342049
NM_000891.2(KCNJ2):c.-2C>T rs144760658
NM_000891.2(KCNJ2):c.-314T>C rs566186294
NM_000891.2(KCNJ2):c.1229A>G (p.Asn410Ser) rs141069645
NM_000891.2(KCNJ2):c.531C>T (p.Gly177=) rs544384907

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