ClinVar Miner

List of variants reported as benign for atrial fibrillation by Illumina Laboratory Services, Illumina

Included ClinVar conditions (49):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_002234.4(KCNA5):c.1149T>C (p.Gly383=) rs2359641 0.98412
NM_000218.3(KCNQ1):c.1393+28111T>G rs114030398 0.56819
NM_000891.3(KCNJ2):c.*1267A>G rs236514 0.52229
NM_002234.4(KCNA5):c.-167C>T rs3741930 0.43501
NM_000218.3(KCNQ1):c.*875A>G rs8234 0.38150
NM_000218.3(KCNQ1):c.*932A>G rs10798 0.37559
NM_002234.4(KCNA5):c.*508A>T rs1056468 0.23863
NM_000218.3(KCNQ1):c.1638G>A (p.Ser546=) rs1057128 0.16286
NM_000218.3(KCNQ1):c.1393+31361T>A rs200391321 0.16051
NM_000891.3(KCNJ2):c.1146C>T (p.Leu382=) rs173135 0.12771
NM_000218.3(KCNQ1):c.*479G>A rs2519184 0.10424
NM_000891.3(KCNJ2):c.*1069C>T rs45603434 0.09819
NM_000218.3(KCNQ1):c.1590+14T>C rs11024034 0.07860
NM_172201.2(KCNE2):c.-79G>A rs41260744 0.07525
NM_000891.3(KCNJ2):c.*624G>A rs9302915 0.07098
NM_000891.3(KCNJ2):c.*558C>T rs9302914 0.06842
NM_000891.3(KCNJ2):c.*136G>A rs73998781 0.06798
NM_000891.3(KCNJ2):c.660C>T (p.Ser220=) rs7221086 0.06793
NM_000891.3(KCNJ2):c.*1198A>G rs9895478 0.06787
NM_000891.3(KCNJ2):c.*1251C>T rs9894661 0.06785
NM_000891.3(KCNJ2):c.*1266C>T rs9894677 0.06783
NM_000891.3(KCNJ2):c.*832G>A rs10083831 0.06743
NM_000218.3(KCNQ1):c.478-10G>A rs28730752 0.04910
NM_002234.4(KCNA5):c.*736A>T rs66942317 0.02811
NM_000891.3(KCNJ2):c.*3496T>C rs3815307 0.01760
NM_172201.2(KCNE2):c.25C>G (p.Gln9Glu) rs16991652 0.00468
NM_000218.3(KCNQ1):c.1343C>G (p.Pro448Arg) rs12720449
NM_000218.3(KCNQ1):c.1986C>T (p.Tyr662=) rs11601907
NM_000891.3(KCNJ2):c.*1678dup rs145779709
NM_000891.3(KCNJ2):c.*640GTT[4] rs397705636
NM_002234.4(KCNA5):c.92G>T (p.Gly31Val) rs61737395

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