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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.3010G>T (p.Ala1004Ser)	rs143978652	0.00110
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn)	rs201307101	0.00024
NM_000218.3(KCNQ1):c.1189C>T (p.Arg397Trp)	rs199472776	0.00013
NM_000441.2(SLC26A4):c.85G>C (p.Glu29Gln)	rs111033205	0.00011
NM_000257.4(MYH7):c.2389G>A (p.Ala797Thr)	rs3218716	0.00003
NM_000257.4(MYH7):c.728G>A (p.Arg243His)	rs267606910	0.00001
NM_000335.5(SCN5A):c.1567C>T (p.Arg523Cys)	rs199473119	0.00001
NM_000218.3(KCNQ1):c.724G>A (p.Asp242Asn)	rs199472712
NM_000335.5(SCN5A):c.1705C>G (p.Arg569Gly)	rs199473576
NM_001232.4(CASQ2):c.2T>C (p.Met1Thr)	rs1553197939
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_005159.5(ACTC1):c.524_525insC (p.Ala176fs)	rs1555418832
NM_020297.4(ABCC9):c.2019+2T>C	rs1555100687

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.