List of variants in gene PPARG reported as pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_138711.6(PPARG):c.1183C>T (p.Arg395Cys)	rs72551364
NM_138711.6(PPARG):c.1271del (p.Pro424fs)	rs770557781
NM_138711.6(PPARG):c.924_928del (p.Asp308fs)	rs1553650477

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