ClinVar Miner

List of variants reported as likely benign for Familial atrial fibrillation

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_005266.6(GJA5):c.-175G>A rs35594137 0.19061
NM_005266.7(GJA5):c.-61A>G rs11552588 0.18395
NM_181703.4(GJA5):c.*608C>T rs36005900 0.14728
NM_002234.3(KCNA5):c.*800G>A rs4625555 0.02358
NM_000218.3(KCNQ1):c.1393+22646C>G rs146407692 0.00925
NM_000218.3(KCNQ1):c.1393+21526C>T rs72847701 0.00923
NM_000218.3(KCNQ1):c.1393+21538C>T rs72850203 0.00923
NM_181703.4(GJA5):c.369C>T (p.Tyr123=) rs2232191 0.00582
NM_000218.3(KCNQ1):c.1514+4974G>A rs188083723 0.00530
NM_000218.3(KCNQ1):c.478-8C>T rs150711844 0.00150
NM_000218.3(KCNQ1):c.*241G>A rs142023323 0.00048
NM_000218.3(KCNQ1):c.1749C>T (p.Arg583=) rs200670744 0.00005
NM_181703.4(GJA5):c.*1396G>A rs886045242 0.00001
NM_000218.3(KCNQ1):c.*377del rs762386874
NM_000218.3(KCNQ1):c.*889AAT[1] rs546360517
NM_005266.6(GJA5):c.-152G= rs791286
NM_020297.4(ABCC9):c.2238-17del rs4148670
NM_181703.4(GJA5):c.*617TGGTATGTACCTCTGGCAAATGCCC[3] rs11267274

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