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

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: 10

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HGVS	dbSNP	gnomAD frequency
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.1258A>C (p.Lys420Gln)	rs587780424
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.520T>C (p.Ser174Pro)	rs2125215217
NM_138711.6(PPARG):c.913G>A (p.Val305Ile)	rs139894525
NM_138711.6(PPARG):c.928A>G (p.Asn310Asp)	rs1274014409
NM_138711.6(PPARG):c.964G>A (p.Glu322Lys)	rs530007199

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