ClinVar Miner

List of variants reported as benign for atrial fibrillation (disease)

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_000891.2(KCNJ2):c.*1069C>T rs45603434
NM_000891.2(KCNJ2):c.*1198A>G rs9895478
NM_000891.2(KCNJ2):c.*1251C>T rs9894661
NM_000891.2(KCNJ2):c.*1267A>G rs236514
NM_000891.2(KCNJ2):c.*136G>A rs73998781
NM_000891.2(KCNJ2):c.*1678dup rs145779709
NM_000891.2(KCNJ2):c.*558C>T rs9302914
NM_000891.2(KCNJ2):c.*624G>A rs9302915
NM_000891.2(KCNJ2):c.*646_*648dupGTT rs397705636
NM_000891.2(KCNJ2):c.*832G>A rs10083831
NM_000891.2(KCNJ2):c.1146C>T (p.Leu382=) rs173135
NM_000891.2(KCNJ2):c.660C>T (p.Ser220=) rs7221086
NM_001148.6(ANK2):c.9854T>C (p.Ile3285Thr) rs36210417
NM_001267550.2(TTN):c.18776C>G (p.Thr6259Ser) rs72648949
NM_001267550.2(TTN):c.47315G>A (p.Arg15772Gln) rs72677233
NM_001267550.2(TTN):c.87877C>T (p.Arg29293Cys) rs191482653
NM_001267550.2(TTN):c.8902+14T>A rs13388274
NM_001267550.2(TTN):c.9359G>A (p.Arg3120Gln) rs72647894
NM_002234.4(KCNA5):c.1149T>C (p.Gly383=) rs2359641
NM_002234.4(KCNA5):c.1353C>T (p.Ala451=) rs767826909
NM_002234.4(KCNA5):c.180G>A (p.Ala60=) rs376660949
NM_002234.4(KCNA5):c.381C>T (p.Ser127=) rs45504599
NM_002234.4(KCNA5):c.751G>A (p.Ala251Thr) rs12720442
NM_004281.3(BAG3):c.1138C>T (p.Pro380Ser) rs144692954
NM_004281.3(BAG3):c.187C>G (p.Pro63Ala) rs144041999
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509
NM_005751.4(AKAP9):c.139C>T (p.His47Tyr) rs35669569
NM_172057.2(KCNH2):c.1670A>C (p.Lys557Thr) rs1805123
NM_181798.1(KCNQ1):c.*479G>A rs2519184
NM_181798.1(KCNQ1):c.*875A>G rs8234
NM_181798.1(KCNQ1):c.*932A>G rs10798
NM_181798.1(KCNQ1):c.1012+28111T>G rs114030398
NM_181798.1(KCNQ1):c.1012+31361T>A rs200391321
NM_181798.1(KCNQ1):c.1257G>A (p.Ser419=) rs1057128
NM_181798.1(KCNQ1):c.1605C>T (p.Tyr535=) rs11601907
NM_181798.1(KCNQ1):c.97-10G>A rs28730752

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