ClinVar Miner

List of variants in gene KCNE2 reported as uncertain significance for atrial fibrillation (disease)

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP
NM_172201.1(KCNE2):c.*240G>C rs773295544
NM_172201.1(KCNE2):c.*62G>A rs72550218
NM_172201.1(KCNE2):c.-121C>T rs188625398
NM_172201.1(KCNE2):c.-13+5G>A rs786205806
NM_172201.1(KCNE2):c.-80C>T rs566735365
NM_172201.1(KCNE2):c.-85G>A rs41315511
NM_172201.1(KCNE2):c.153G>T (p.Leu51=) rs143767851
NM_172201.1(KCNE2):c.354G>A (p.Gly118=) rs187917779
NM_172201.1(KCNE2):c.79C>T (p.Arg27Cys) rs74315449
NM_172201.2(KCNE2):c.*11A>C
NM_172201.2(KCNE2):c.*234G>A
NM_172201.2(KCNE2):c.*61C>T
NM_172201.2(KCNE2):c.178T>A (p.Phe60Ile)
NM_172201.2(KCNE2):c.17A>G (p.Asn6Ser)

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