ClinVar Miner

List of variants reported as benign for Epilepsy, idiopathic generalized, susceptibility to, 13 by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001127644.2(GABRA1):c.1059+15G>A rs2279020 0.62825
NM_001127644.2(GABRA1):c.*470A>G rs2290732 0.59993
NM_001127644.2(GABRA1):c.*1506A>C rs998754 0.59915
NM_000806.5(GABRA1):c.-441A>G rs11576001 0.29650
NM_001127644.2(GABRA1):c.156T>C (p.Gly52=) rs1129647 0.23538
NM_001127644.2(GABRA1):c.-142A>G rs12658835 0.18507
NM_001127644.2(GABRA1):c.-31C>T rs4608967 0.13578
NM_001127644.2(GABRA1):c.*1929T>C rs2290733 0.01265

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.