| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129936198, LOC129936199 +647 more | Copy number gain | See cases | |
| | LOC129936421, LOC129936422 +962 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC110120630, LOC111429626 +608 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +307 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +190 more | Copy number gain | See cases | |
| | LOC132088948, LOC132088950 +730 more | Copy number gain | See cases | |
| | | Single nucleotide variant (intron variant) | Type 2 diabetes mellitus | |
| | | Single nucleotide variant (intron variant) | Type 2 diabetes mellitus | |
| | | Single nucleotide variant (intron variant) | Type 2 diabetes mellitus | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Obesity +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +2 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Deletion (frameshift variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (5 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) | Diabetes mellitus, noninsulin-dependent, modifier of +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Deletion (frameshift variant +1 more) | Obesity | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Obesity +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inherited obesity | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Obesity +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (nonsense +1 more) | PPARG-related familial partial lipodystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | 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 | |
| | | 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) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related familial partial lipodystrophy +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder | |
| | | Duplication (frameshift variant +1 more) | PPARG-related familial partial lipodystrophy +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related familial partial lipodystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related familial partial lipodystrophy | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | PPARG-related disorder | |
| | | Single nucleotide variant (intron variant) | Obesity +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | Obesity +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PPARG-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | Obesity +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | PPARG-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |