ClinVar Miner

List of variants in gene KCNQ2 reported as benign

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Gene type:
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Total variants: 74
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HGVS dbSNP
GRCh37/hg19 20q13.33(chr20:62075098-62119121)x4
NM_172107.3(KCNQ2):c.*248C>T rs6122440
NM_172107.3(KCNQ2):c.*295C>T rs34690549
NM_172107.3(KCNQ2):c.*4G>A rs1801508
NM_172107.3(KCNQ2):c.-11C>T rs182089624
NM_172107.3(KCNQ2):c.-46C>G rs572005014
NM_172107.3(KCNQ2):c.-88G>T rs185287315
NM_172107.3(KCNQ2):c.1023+9A>G rs201787699
NM_172107.3(KCNQ2):c.1053C>T (p.Leu351=) rs1030017847
NM_172107.3(KCNQ2):c.1065C>T (p.Asp355=) rs200395340
NM_172107.3(KCNQ2):c.1118+69C>A rs142571798
NM_172107.3(KCNQ2):c.1118+69C>T rs142571798
NM_172107.3(KCNQ2):c.1149-20C>T rs754997316
NM_172107.3(KCNQ2):c.1161G>A (p.Pro387=) rs147453497
NM_172107.3(KCNQ2):c.1185G>A (p.Arg395=) rs35430888
NM_172107.3(KCNQ2):c.1270C>T (p.Pro424Ser) rs748120886
NM_172107.3(KCNQ2):c.1301+7C>T rs374877247
NM_172107.3(KCNQ2):c.1302-11C>G rs371007020
NM_172107.3(KCNQ2):c.1302-11C>T rs371007020
NM_172107.3(KCNQ2):c.1302-18_1302-17insCGTCTGTC rs1555854857
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGCCTGTC rs1555854856
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCCGTC rs1555854855
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCTCTC rs1555854853
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCTGAC rs1555854852
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCTGCC rs1555854852
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCTGTT rs1555854850
NM_172107.3(KCNQ2):c.1302-18_1302-17insTGTCTTTC rs1555854853
NM_172107.3(KCNQ2):c.1302-20_1302-19insCCTGTCTG rs796052609
NM_172107.3(KCNQ2):c.1302-25_1302-18dup rs112006486
NM_172107.3(KCNQ2):c.1348G>A (p.Val450Met) rs146492238
NM_172107.3(KCNQ2):c.1407C>T (p.Ala469=) rs1801385
NM_172107.3(KCNQ2):c.1419C>T (p.Leu473=) rs370155790
NM_172107.3(KCNQ2):c.1458C>T (p.Phe486=) rs141951341
NM_172107.3(KCNQ2):c.1503C>G (p.Ala501=) rs1801545
NM_172107.3(KCNQ2):c.1539C>T (p.Pro513=) rs376713245
NM_172107.3(KCNQ2):c.1545G>C (p.Glu515Asp) rs117067974
NM_172107.3(KCNQ2):c.1602G>A (p.Pro534=) rs775089685
NM_172107.3(KCNQ2):c.1632-18C>A rs368910668
NM_172107.3(KCNQ2):c.1689C>T (p.Asp563=) rs35450031
NM_172107.3(KCNQ2):c.1719C>T (p.Ala573=) rs61737409
NM_172107.3(KCNQ2):c.1763+17C>A rs548507063
NM_172107.3(KCNQ2):c.1827C>T (p.Ala609=) rs369438374
NM_172107.3(KCNQ2):c.1833G>A (p.Ala611=) rs564630217
NM_172107.3(KCNQ2):c.1887+16C>A rs369329706
NM_172107.3(KCNQ2):c.1887+17G>A rs369457896
NM_172107.3(KCNQ2):c.1956G>A (p.Pro652=) rs749070370
NM_172107.3(KCNQ2):c.2031G>A (p.Arg677=) rs35647984
NM_172107.3(KCNQ2):c.2065A>C (p.Ile689Leu) rs201701585
NM_172107.3(KCNQ2):c.2087C>T (p.Thr696Met) rs570139975
NM_172107.3(KCNQ2):c.2106G>A (p.Ser702=) rs187252584
NM_172107.3(KCNQ2):c.2235G>A (p.Pro745=) rs139587368
NM_172107.3(KCNQ2):c.2238T>A (p.Pro746=) rs1801471
NM_172107.3(KCNQ2):c.2264A>G (p.Tyr755Cys) rs3746366
NM_172107.3(KCNQ2):c.2339A>C (p.Asn780Thr) rs1801475
NM_172107.3(KCNQ2):c.2385C>T (p.His795=) rs143016981
NM_172107.3(KCNQ2):c.2529C>T (p.Ser843=) rs140674819
NM_172107.3(KCNQ2):c.2535C>G (p.Leu845=) rs199621855
NM_172107.3(KCNQ2):c.2544G>A (p.Pro848=) rs147274045
NM_172107.3(KCNQ2):c.2556G>A (p.Pro852=) rs3810472
NM_172107.3(KCNQ2):c.2560C>T (p.Arg854Cys) rs373536274
NM_172107.3(KCNQ2):c.2564C>T (p.Ser855Leu) rs12481082
NM_172107.3(KCNQ2):c.2571C>T (p.Thr857=) rs764525788
NM_172107.3(KCNQ2):c.297-18C>T rs370109710
NM_172107.3(KCNQ2):c.303C>G (p.Leu101=) rs145415996
NM_172107.3(KCNQ2):c.515-9G>A rs755243604
NM_172107.3(KCNQ2):c.570C>T (p.Asn190=) rs116087798
NM_172107.3(KCNQ2):c.714C>T (p.Ile238=) rs147882199
NM_172107.3(KCNQ2):c.754T>C (p.Leu252=) rs370174915
NM_172107.3(KCNQ2):c.774C>T (p.Asn258=) rs770187706
NM_172107.3(KCNQ2):c.804C>T (p.Leu268=) rs775450377
NM_172107.3(KCNQ2):c.816+10G>T rs201012161
NM_172107.3(KCNQ2):c.81G>A (p.Leu27=) rs373897282
NM_172107.3(KCNQ2):c.888C>T (p.Thr296=) rs370760854
NM_172107.3(KCNQ2):c.912C>T (p.Phe304=) rs2297385

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