ClinVar Miner

List of variants reported as likely pathogenic for Wolff-Parkinson-White pattern

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Total variants: 15
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HGVS dbSNP
NM_000257.4(MYH7):c.2389G>A (p.Ala797Thr) rs3218716
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn) rs201307101
NM_000257.4(MYH7):c.728G>A (p.Arg243His) rs267606910
NM_000441.2(SLC26A4):c.85G>C (p.Glu29Gln) rs111033205
NM_001267550.2(TTN):c.66904C>T (p.Leu22302=) rs1553624186
NM_001267550.2(TTN):c.92683C>T (p.Arg30895Ter) rs869312065
NM_001276345.2(TNNT2):c.3G>A (p.Met1Ile) rs1289914935
NM_002230.4(JUP):c.773A>G (p.Glu258Gly) rs794729052
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser) rs143978652
NM_005159.5(ACTC1):c.524_525insC (p.Ala176fs) rs1555418832
NM_005691.3(ABCC9):c.2019+2T>C rs1555100687
NM_181798.1(KCNQ1):c.343G>A (p.Asp115Asn) rs199472712
NM_181798.1(KCNQ1):c.808C>T (p.Arg270Trp) rs199472776
NM_198056.2(SCN5A):c.1567C>T (p.Arg523Cys) rs199473119
NM_198056.2(SCN5A):c.1705C>G (p.Arg569Gly) rs199473576

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