List of variants reported as likely benign for Jervell and Lange-Nielsen syndrome 1

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.*975C>T	rs74048340	0.00794
NM_000218.3(KCNQ1):c.1927G>A (p.Gly643Ser)	rs1800172	0.00760
NM_000218.3(KCNQ1):c.720C>T (p.His240=)	rs28730754	0.00524
NM_000218.3(KCNQ1):c.1222C>G (p.Pro408Ala)	rs28730756	0.00447
NM_000218.3(KCNQ1):c.*464G>A	rs141960532	0.00438
NM_000218.3(KCNQ1):c.*731G>A	rs146324627	0.00335
NM_000218.3(KCNQ1):c.435C>T (p.Ile145=)	rs1800170	0.00158
NM_000218.3(KCNQ1):c.1332G>A (p.Thr444=)	rs144985256	0.00054
NM_000218.3(KCNQ1):c.1179G>T (p.Lys393Asn)	rs12720457	0.00053
NM_000218.3(KCNQ1):c.1431C>T (p.Pro477=)	rs137887424	0.00050
NM_000218.3(KCNQ1):c.972C>T (p.Val324=)	rs554518844	0.00047
NM_000218.3(KCNQ1):c.1794+11G>A	rs186188610	0.00029
NM_000218.3(KCNQ1):c.1110G>A (p.Ala370=)	rs1805118	0.00014
NM_000218.3(KCNQ1):c.567G>T (p.Gly189=)	rs200669271	0.00014
NM_000218.3(KCNQ1):c.1458C>T (p.Ala486=)	rs200275211	0.00009
NM_000218.3(KCNQ1):c.1749C>T (p.Arg583=)	rs200670744	0.00005
NM_000218.3(KCNQ1):c.1795-10G>A	rs780067234	0.00002
NM_000218.3(KCNQ1):c.345G>A (p.Glu115=)	rs758960211	0.00002
NM_000218.3(KCNQ1):c.*806C>T	rs539398869	0.00001
NM_000218.3(KCNQ1):c.1377C>T (p.Asp459=)	rs200418488	0.00001
NM_000218.3(KCNQ1):c.1686-18C>G	rs1846715620	0.00001
NM_000218.3(KCNQ1):c.604+12C>T	rs370821907	0.00001
NM_000218.3(KCNQ1):c.*632C>T	rs568824453
NM_000218.3(KCNQ1):c.1875C>T (p.Pro625=)	rs112113213
NM_000218.3(KCNQ1):c.207G>T (p.Ala69=)	rs587781009
NM_000218.3(KCNQ1):c.513C>T (p.Tyr171=)	rs139042529

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