ClinVar Miner

List of variants in gene PRDM8 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_020226.3(PRDM8):c.1314C>T (p.Ala438=) rs188061449
NM_020226.3(PRDM8):c.1674T>C (p.Gly558=) rs774459714
NM_020226.3(PRDM8):c.1812G>A (p.Gln604=) rs1553906523
NM_020226.3(PRDM8):c.1968C>G (p.Pro656=) rs547453696
NM_020226.3(PRDM8):c.654G>A (p.Glu218=) rs1553905625
NM_020226.3(PRDM8):c.985C>T (p.Leu329=) rs560049733

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.