ClinVar Miner

List of variants in gene PRKAG2 reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016203.4(PRKAG2):c.-90G>T rs76351165 0.05040
NM_016203.4(PRKAG2):c.*452C>T rs17714947 0.03769
NM_016203.4(PRKAG2):c.*3G>A rs113234987 0.00973
NM_016203.4(PRKAG2):c.*384C>T rs75418446 0.00847
NM_016203.4(PRKAG2):c.*56G>A rs141781827 0.00626
NM_016203.4(PRKAG2):c.*572G>A rs78192883 0.00384
NM_016203.4(PRKAG2):c.1593G>A (p.Arg531=) rs148197254 0.00374
NM_016203.4(PRKAG2):c.111T>A (p.Ile37=) rs144426409 0.00259
NM_016203.4(PRKAG2):c.1098A>G (p.Pro366=) rs116541276 0.00169
NM_016203.4(PRKAG2):c.1704G>A (p.Thr568=) rs138167675 0.00150
NM_016203.4(PRKAG2):c.298G>A (p.Gly100Ser) rs79474211 0.00144
NM_016203.4(PRKAG2):c.*135T>C rs184932311 0.00041
NM_016203.4(PRKAG2):c.*1021del rs11329945
NM_016203.4(PRKAG2):c.*399G>A rs112179332
NM_016203.4(PRKAG2):c.-287C>G rs75059373

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.