| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (nonsense) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (nonsense) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Inherited obesity | |
| | | Single nucleotide variant (missense variant) | Inherited obesity | |
| | | Duplication (frameshift variant) | Inherited obesity | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | GPATCH3, LOC129929851 +1 more (E9Q) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Obesity | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | NR0B2-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Obesity | |
| | | Deletion (frameshift variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Indel (frameshift variant) | Obesity | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | NR0B2-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | Obesity, mild, early-onset | |