ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
Download table as spreadsheet
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.