ClinVar Miner

List of variants in gene KCNQ4 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_004700.4(KCNQ4):c.708+14G>C rs2361660 0.66283
NM_004700.4(KCNQ4):c.708+175T>G rs2885330 0.65644
NM_004700.4(KCNQ4):c.708+54A>G rs2361659 0.65636
NM_004700.4(KCNQ4):c.777T>C (p.Ala259=) rs4660468 0.65097
NM_004700.4(KCNQ4):c.708+168A>G rs2361657 0.65007
NM_004700.4(KCNQ4):c.1745+249T>C rs729589 0.44322
NM_004700.4(KCNQ4):c.1131-190C>T rs3767939 0.32223
NM_004700.4(KCNQ4):c.1514-176G>A rs874847 0.25480
NM_004700.4(KCNQ4):c.709-155G>A rs12145930 0.22136
NM_004700.4(KCNQ4):c.1365T>G (p.His455Gln) rs34287852 0.16693
NM_004700.4(KCNQ4):c.315-18C>T rs13374844 0.15653
NM_004700.4(KCNQ4):c.533-58C>G rs2296838 0.15446
NM_004700.4(KCNQ4):c.315-16C>T rs13374845 0.15351
NM_004700.4(KCNQ4):c.1745+264G>C rs727334 0.14647
NM_004700.4(KCNQ4):c.1745+182C>A rs729590 0.14100
NM_004700.4(KCNQ4):c.834+27C>A rs33932028 0.12769
NM_004700.4(KCNQ4):c.1614-213C>T rs35608423 0.11845
NM_004700.4(KCNQ4):c.1876-79G>A rs12740352 0.10862
NM_004700.4(KCNQ4):c.873G>A (p.Pro291=) rs12117176 0.08007
NM_004700.4(KCNQ4):c.879A>G (p.Thr293=) rs12143503 0.07598
NM_004700.4(KCNQ4):c.1130+31G>C rs148218398 0.07323
NM_004700.4(KCNQ4):c.1745+256G>C rs6676655 0.06601
NM_004700.4(KCNQ4):c.1614-103G>A rs34480358 0.06313
NM_004700.4(KCNQ4):c.1613+73A>G rs74071723 0.05650
NM_004700.4(KCNQ4):c.708+121C>T rs116688226 0.05419
NM_004700.4(KCNQ4):c.1613+125G>A rs55916242 0.05266
NM_004700.4(KCNQ4):c.*111A>G rs55862109 0.04970
NM_004700.4(KCNQ4):c.834+151A>G rs11810608 0.04448
NM_004700.4(KCNQ4):c.1665G>A (p.Pro555=) rs55964611 0.03837
NM_004700.4(KCNQ4):c.841T>C (p.Leu281=) rs55737429 0.03713
NM_004700.4(KCNQ4):c.1657C>T (p.Leu553=) rs55925184 0.03211
NM_004700.4(KCNQ4):c.709-209G>C rs12097892 0.02220
NM_004700.4(KCNQ4):c.1986C>G (p.Pro662=) rs191631836 0.00145
NM_004700.4(KCNQ4):c.1818C>G (p.Asp606Glu) rs139835231 0.00129
NM_004700.4(KCNQ4):c.972G>A (p.Leu324=) rs137896524 0.00085
NM_004700.4(KCNQ4):c.946-12C>G rs146802754 0.00057
NM_004700.4(KCNQ4):c.1130+28T>G rs376712113
NM_004700.4(KCNQ4):c.1292+305C>T rs3767941
NM_004700.4(KCNQ4):c.1292+63T>C rs3767940
NM_004700.4(KCNQ4):c.1514-136dup rs5773705
NM_004700.4(KCNQ4):c.1514-34T>C rs913378
NM_004700.4(KCNQ4):c.1614-217C>T rs72661521
NM_004700.4(KCNQ4):c.708+157C>G rs2361658
NM_004700.4(KCNQ4):c.709-185A>T rs45536233
NM_004700.4(KCNQ4):c.834+148C>A rs35493687

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