List of variants reported as likely benign for Myokymia

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000217.3(KCNA1):c.*2308C>G	rs114342545	0.01314
NM_000217.3(KCNA1):c.*1892C>T	rs146972463	0.00806
NM_000217.3(KCNA1):c.*3840G>A	rs148103166	0.00509
NM_000217.3(KCNA1):c.*127A>C	rs116918891	0.00476
NM_000217.3(KCNA1):c.*189G>A	rs187069793	0.00226
NM_000217.3(KCNA1):c.-235C>A	rs113587682	0.00086
NM_000217.3(KCNA1):c.*923T>C	rs142134789	0.00076
NM_000217.3(KCNA1):c.*2313C>T	rs183989674	0.00022
NM_000217.3(KCNA1):c.*4663G>A	rs186319441	0.00022
NM_000217.3(KCNA1):c.*5191G>A	rs575078827	0.00002
NM_000217.3(KCNA1):c.*1444CAAA[6]	rs138257860
NM_000217.3(KCNA1):c.-478dup	rs34346629
NM_000217.3(KCNA1):c.-865AG[2]	rs566173456

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.