ClinVar Miner

List of variants in gene KCNQ2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 25
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HGVS dbSNP
NM_172107.4(KCNQ2):c.*110G>A rs141692577
NM_172107.4(KCNQ2):c.*421C>T rs578175518
NM_172107.4(KCNQ2):c.*4G>A rs1801508
NM_172107.4(KCNQ2):c.-11C>T rs182089624
NM_172107.4(KCNQ2):c.-150C>A rs554261385
NM_172107.4(KCNQ2):c.-42G>T rs577705653
NM_172107.4(KCNQ2):c.1065C>T (p.Asp355=) rs200395340
NM_172107.4(KCNQ2):c.1253G>T (p.Gly418Val) rs201750561
NM_172107.4(KCNQ2):c.1348G>A (p.Val450Met) rs146492238
NM_172107.4(KCNQ2):c.1458C>T (p.Phe486=) rs141951341
NM_172107.4(KCNQ2):c.1545G>C (p.Glu515Asp) rs117067974
NM_172107.4(KCNQ2):c.1689C>T (p.Asp563=) rs35450031
NM_172107.4(KCNQ2):c.1719C>T (p.Ala573=) rs61737409
NM_172107.4(KCNQ2):c.1827C>T (p.Ala609=) rs369438374
NM_172107.4(KCNQ2):c.2031G>A (p.Arg677=) rs35647984
NM_172107.4(KCNQ2):c.2065A>C (p.Ile689Leu) rs201701585
NM_172107.4(KCNQ2):c.2106G>A (p.Ser702=) rs187252584
NM_172107.4(KCNQ2):c.2529C>T (p.Ser843=) rs140674819
NM_172107.4(KCNQ2):c.2544G>A (p.Pro848=) rs147274045
NM_172107.4(KCNQ2):c.2556G>A (p.Pro852=) rs3810472
NM_172107.4(KCNQ2):c.691-13G>A rs547887704
NM_172107.4(KCNQ2):c.741G>A (p.Ser247=) rs184792288
NM_172107.4(KCNQ2):c.754T>C (p.Leu252=) rs370174915
NM_172107.4(KCNQ2):c.81G>A (p.Leu27=) rs373897282
NM_172107.4(KCNQ2):c.888C>T (p.Thr296=) rs370760854

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