ClinVar Miner

List of variants in gene KCNE2, LOC105372791 studied for atrial fibrillation

Included ClinVar conditions (51):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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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.-13+5G>A rs786205806 0.00043
NM_172201.2(KCNE2):c.*62G>A rs72550218 0.00034
NM_172201.2(KCNE2):c.80G>A (p.Arg27His) rs148968498 0.00025
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.346G>A (p.Ala116Thr) rs150790888 0.00009
NM_172201.2(KCNE2):c.369_370del (p.Ter124IleextTer?) rs45610936 0.00009
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.228A>G (p.Arg76=) rs202169020 0.00004
NM_172201.2(KCNE2):c.229C>T (p.Arg77Trp) rs141423405 0.00004
NM_172201.2(KCNE2):c.67A>T (p.Met23Leu) rs747045005 0.00004
NM_172201.2(KCNE2):c.-121C>T rs188625398 0.00003
NM_172201.2(KCNE2):c.-80C>T rs566735365 0.00002
NM_172201.2(KCNE2):c.204G>A (p.Leu68=) rs200403369 0.00002
NM_172201.2(KCNE2):c.144dup (p.Val49fs) rs751276927 0.00001
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.242A>G (p.Asn81Ser) rs1434304789 0.00001
NM_172201.2(KCNE2):c.2T>C (p.Met1Thr) rs867658122 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
NM_172201.2(KCNE2):c.13T>C (p.Ser5Pro) rs2123423458
NM_172201.2(KCNE2):c.193G>C (p.Val65Leu) rs199473364
NM_172201.2(KCNE2):c.269A>G (p.Glu90Gly) rs199473366

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