ClinVar Miner

List of variants in gene KCNQ3 reported as uncertain significance by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
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Total variants: 18
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NM_004519.4(KCNQ3):c.1226C>G (p.Pro409Arg) rs149272208
NM_004519.4(KCNQ3):c.127G>A (p.Val43Met) rs794726918
NM_004519.4(KCNQ3):c.1403A>G (p.Asn468Ser) rs118192252
NM_004519.4(KCNQ3):c.1458T>A (p.Ser486Arg) rs886043116
NM_004519.4(KCNQ3):c.1529A>C (p.Asp510Ala) rs1554622841
NM_004519.4(KCNQ3):c.1543C>G (p.Leu515Val) rs368013249
NM_004519.4(KCNQ3):c.154C>G (p.Gln52Glu) rs1327292650
NM_004519.4(KCNQ3):c.1564G>A (p.Val522Ile) rs143683496
NM_004519.4(KCNQ3):c.1722T>C (p.Pro574=) rs1554622049
NM_004519.4(KCNQ3):c.1935A>G (p.Gln645=) rs587781011
NM_004519.4(KCNQ3):c.1994C>T (p.Ser665Leu) rs147173555
NM_004519.4(KCNQ3):c.2330G>A (p.Arg777Gln) rs201328910
NM_004519.4(KCNQ3):c.2391C>T (p.His797=) rs763446963
NM_004519.4(KCNQ3):c.2462A>G (p.Asn821Ser) rs118192254
NM_004519.4(KCNQ3):c.604+10G>T rs541587196
NM_004519.4(KCNQ3):c.788C>T (p.Thr263Met) rs1479652323
NM_004519.4(KCNQ3):c.867G>A (p.Val289=)
NM_004519.4(KCNQ3):c.954C>A (p.Gly318=) rs143224896

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