List of variants reported as uncertain significance for atrial fibrillation, familial, 4

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
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.-13+5G>A	rs786205806	0.00013
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.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

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