ClinVar Miner

List of variants in gene PPARG reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_138711.6(PPARG):c.1341C>T (p.His447=) rs3856806 0.11181
NM_138711.6(PPARG):c.-8-28078C>G rs1801282 0.08816
NM_138711.6(PPARG):c.1362C>T (p.Ile454=) rs149367249 0.00250
NM_138711.6(PPARG):c.913G>C (p.Val305Leu) rs139894525 0.00135
NM_138711.6(PPARG):c.348T>C (p.Ala116=) rs147975759 0.00056
NM_138711.6(PPARG):c.145G>A (p.Glu49Lys) rs777334819 0.00003
NM_138711.6(PPARG):c.1064G>A (p.Arg355Gln) rs140204299 0.00001
NM_138711.6(PPARG):c.1206G>C (p.Lys402Asn) rs1437186245 0.00001
NM_138711.6(PPARG):c.1045G>A (p.Glu349Lys) rs1553650533
NM_138711.6(PPARG):c.1183C>T (p.Arg395Cys) rs72551364
NM_138711.6(PPARG):c.1258A>C (p.Lys420Gln) rs587780424
NM_138711.6(PPARG):c.1262T>C (p.Leu421Pro) rs1553653993
NM_138711.6(PPARG):c.1271del (p.Pro424fs) rs770557781
NM_138711.6(PPARG):c.380A>G (p.Glu127Gly) rs1553643326
NM_138711.6(PPARG):c.392G>T (p.Gly131Val) rs1553645235
NM_138711.6(PPARG):c.452G>A (p.Arg151Gln) rs2050121670
NM_138711.6(PPARG):c.491G>A (p.Arg164Gln) rs148195788
NM_138711.6(PPARG):c.520T>C (p.Ser174Pro) rs2125215217
NM_138711.6(PPARG):c.801C>G (p.Pro267=) rs13306747
NM_138711.6(PPARG):c.881T>C (p.Ile294Thr) rs1378972597
NM_138711.6(PPARG):c.913G>A (p.Val305Ile) rs139894525
NM_138711.6(PPARG):c.920T>C (p.Leu307Pro) rs2125284643
NM_138711.6(PPARG):c.924_928del (p.Asp308fs) rs1553650477
NM_138711.6(PPARG):c.928A>G (p.Asn310Asp) rs1274014409
NM_138711.6(PPARG):c.964G>A (p.Glu322Lys) rs530007199

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.