| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related familial partial lipodystrophy +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Duplication (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related familial partial lipodystrophy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Obesity +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | LOC114803475, PPARG (A263V +2 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | LOC114803475, PPARG (I234T +2 more) | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | LOC114803475, PPARG (E256fs +1 more) | Duplication (frameshift variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Obesity +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | PPARG-related disorder | |