ClinVar Miner

List of variants in gene KCNQ1 reported as uncertain significance for Romano-Ward syndrome

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Total variants: 33
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HGVS dbSNP
NM_000218.2(KCNQ1):c.*1025G>C rs181226788
NM_000218.2(KCNQ1):c.*1055C>T rs375155898
NM_000218.2(KCNQ1):c.*1088G>C rs886048177
NM_000218.2(KCNQ1):c.*160C>A rs886048167
NM_000218.2(KCNQ1):c.*171G>A rs886048168
NM_000218.2(KCNQ1):c.*26C>A rs886048166
NM_000218.2(KCNQ1):c.*292C>A rs886048169
NM_000218.2(KCNQ1):c.*391G>A rs774059974
NM_000218.2(KCNQ1):c.*392A>C rs868129989
NM_000218.2(KCNQ1):c.*398C>T rs886048170
NM_000218.2(KCNQ1):c.*47A>C rs754931159
NM_000218.2(KCNQ1):c.*539G>C rs886048171
NM_000218.2(KCNQ1):c.*554T>G rs886048172
NM_000218.2(KCNQ1):c.*581T>C rs765566577
NM_000218.2(KCNQ1):c.*633G>A rs886048173
NM_000218.2(KCNQ1):c.*652G>A rs886048174
NM_000218.2(KCNQ1):c.*712G>A rs745447199
NM_000218.2(KCNQ1):c.*877C>G rs763163556
NM_000218.2(KCNQ1):c.*887_*889delTCA rs886048175
NM_000218.2(KCNQ1):c.*897G>T rs561861522
NM_000218.2(KCNQ1):c.-38C>T rs886048160
NM_000218.2(KCNQ1):c.-69G>A rs886048159
NM_000218.2(KCNQ1):c.1189C>T (p.Arg397Trp) rs199472776
NM_000218.2(KCNQ1):c.1251+13C>T rs201364493
NM_000218.2(KCNQ1):c.1355G>A (p.Arg452Gln) rs145229963
NM_000218.2(KCNQ1):c.1794+12C>T rs727505084
NM_000218.2(KCNQ1):c.1973C>A (p.Thr658Asn) rs377661455
NM_000218.2(KCNQ1):c.1979C>A (p.Pro660His) rs886048165
NM_000218.2(KCNQ1):c.29C>A (p.Ala10Asp) rs886048161
NM_000218.2(KCNQ1):c.387-7C>T rs201682200
NM_000218.2(KCNQ1):c.650C>T (p.Ser217Phe) rs886048163
NM_000218.2(KCNQ1):c.66C>T (p.Gly22=) rs886048162
NM_000218.2(KCNQ1):c.781-6G>T rs886048164

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