ClinVar Miner

List of variants studied for atrial fibrillation, familial, 4 by Illumina Laboratory Services, Illumina

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_172201.2(KCNE2):c.-79G>A rs41260744 0.07525
NM_172201.2(KCNE2):c.-52G>A rs41314699 0.00570
NM_172201.2(KCNE2):c.25C>G (p.Gln9Glu) rs16991652 0.00468
NM_172201.2(KCNE2):c.170T>C (p.Ile57Thr) rs74315448 0.00063
NM_172201.2(KCNE2):c.*62G>A rs72550218 0.00034
NM_172201.2(KCNE2):c.153G>T (p.Leu51=) rs143767851 0.00019
NM_172201.2(KCNE2):c.354G>A (p.Gly118=) rs187917779 0.00019
NM_172201.2(KCNE2):c.-13+5G>A rs786205806 0.00013
NM_172201.2(KCNE2):c.79C>T (p.Arg27Cys) rs74315449 0.00006
NM_172201.2(KCNE2):c.*234G>A rs981526333 0.00004
NM_172201.2(KCNE2):c.-85G>A rs41315511 0.00004
NM_172201.2(KCNE2):c.-80C>T rs566735365 0.00002
NM_172201.2(KCNE2):c.178T>A (p.Phe60Ile) rs16991654 0.00001
NM_172201.2(KCNE2):c.17A>G (p.Asn6Ser) rs776661633 0.00001
NM_172201.2(KCNE2):c.*11A>C rs558860396
NM_172201.2(KCNE2):c.*240G>C rs773295544
NM_172201.2(KCNE2):c.*61C>T rs551483595

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