ClinVar Miner

List of variants in gene KCNQ1 reported as likely benign for Romano-Ward syndrome

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Gene type:
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Total variants: 36
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HGVS dbSNP
NM_000218.2(KCNQ1):c.*219G>A rs45477500
NM_000218.2(KCNQ1):c.*241G>A rs142023323
NM_000218.2(KCNQ1):c.*264T>C rs45579540
NM_000218.2(KCNQ1):c.*266G>A rs113029000
NM_000218.2(KCNQ1):c.*305A>C rs45570140
NM_000218.2(KCNQ1):c.*350G>A rs114877430
NM_000218.2(KCNQ1):c.*377delG rs762386874
NM_000218.2(KCNQ1):c.*411C>T rs45460605
NM_000218.2(KCNQ1):c.*464G>A rs141960532
NM_000218.2(KCNQ1):c.*482G>A rs45510192
NM_000218.2(KCNQ1):c.*717T>G rs189162344
NM_000218.2(KCNQ1):c.*731G>A rs146324627
NM_000218.2(KCNQ1):c.*742G>A rs114844136
NM_000218.2(KCNQ1):c.*806C>T rs539398869
NM_000218.2(KCNQ1):c.*837G>A rs139633955
NM_000218.2(KCNQ1):c.*892_*894delAAT rs546360517
NM_000218.2(KCNQ1):c.*904T>C rs186055804
NM_000218.2(KCNQ1):c.*975C>T rs74048340
NM_000218.2(KCNQ1):c.-5T>C rs532941548
NM_000218.2(KCNQ1):c.1110G>A (p.Ala370=) rs1805118
NM_000218.2(KCNQ1):c.1179G>T (p.Lys393Asn) rs12720457
NM_000218.2(KCNQ1):c.1222C>G (p.Pro408Ala) rs28730756
NM_000218.2(KCNQ1):c.1590+14T>C rs11024034
NM_000218.2(KCNQ1):c.1749C>T (p.Arg583=) rs200670744
NM_000218.2(KCNQ1):c.1794+11G>A rs186188610
NM_000218.2(KCNQ1):c.1875C>T (p.Pro625=) rs112113213
NM_000218.2(KCNQ1):c.1927G>A (p.Gly643Ser) rs1800172
NM_000218.2(KCNQ1):c.1942G>A (p.Val648Ile) rs34150427
NM_000218.2(KCNQ1):c.207G>T (p.Ala69=) rs587781009
NM_000218.2(KCNQ1):c.435C>T (p.Ile145=) rs1800170
NM_000218.2(KCNQ1):c.459G>A (p.Thr153=) rs148121889
NM_000218.2(KCNQ1):c.477+9C>T rs28730664
NM_000218.2(KCNQ1):c.478-8C>T rs150711844
NM_000218.2(KCNQ1):c.513C>T (p.Tyr171=) rs139042529
NM_000218.2(KCNQ1):c.720C>T (p.His240=) rs28730754
NM_000218.2(KCNQ1):c.972C>T (p.Val324=) rs554518844

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