ClinVar Miner

List of variants in gene KCNQ2 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_172107.3(KCNQ2):c.2252C>T (p.Ser751Leu) rs774002673
NM_172107.4(KCNQ2):c.*412C>T rs886056920
NM_172107.4(KCNQ2):c.*413G>A rs886056919
NM_172107.4(KCNQ2):c.-107G>A rs886056923
NM_172107.4(KCNQ2):c.-169G>T rs886056924
NM_172107.4(KCNQ2):c.-83G>T rs886056922
NM_172107.4(KCNQ2):c.1281A>G (p.Gly427=) rs781056597
NM_172107.4(KCNQ2):c.185C>G (p.Ala62Gly) rs796052612
NM_172107.4(KCNQ2):c.2049C>T (p.His683=) rs150982653
NM_172107.4(KCNQ2):c.2209G>A (p.Gly737Ser) rs755013341
NM_172107.4(KCNQ2):c.2469C>T (p.Ala823=) rs758071891
NM_172107.4(KCNQ2):c.387+9C>T rs751969586
NM_172107.4(KCNQ2):c.691-5C>T rs886056921
NM_172107.4(KCNQ2):c.816+9T>C rs772235691
NM_172107.4(KCNQ2):c.900C>T (p.Ile300=) rs764404303

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