List of variants in gene PRICKLE2 reported as likely benign for adolescent-onset epilepsy syndrome

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

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_198859.4(PRICKLE2):c.-252G>C	rs142388795	0.01230
NM_198859.4(PRICKLE2):c.*3489G>A	rs143062140	0.00811
NM_198859.4(PRICKLE2):c.*3852C>A	rs153731	0.00717
NM_198859.4(PRICKLE2):c.1527G>A (p.Glu509=)	rs144455095	0.00228
NM_198859.4(PRICKLE2):c.*4057G>A	rs140931283	0.00204
NM_198859.4(PRICKLE2):c.444C>T (p.Arg148=)	rs146538069	0.00190
NM_198859.4(PRICKLE2):c.788-6T>C	rs180903875	0.00143
NM_198859.4(PRICKLE2):c.*133G>A	rs370569305	0.00021
NM_198859.4(PRICKLE2):c.*4354C>G	rs186186236	0.00017
NM_198859.4(PRICKLE2):c.*2633G>A	rs140420417	0.00003
NM_198859.4(PRICKLE2):c.*2269T>C	rs550841859	0.00002
NM_198859.4(PRICKLE2):c.*3178G>C	rs528929996	0.00002

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.