| | CCDC146, CCDC201 +4735 more | Copy number loss | See cases | |
| | LOC129998995, LOC129998996 +2212 more | Copy number gain | See cases | |
| | LOC129999548, LOC129999549 +1547 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129999315, LOC129999316 +342 more | Copy number loss | See cases | |
| | LOC129999254, LOC129999255 +284 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (5 prime UTR variant) | Monogenic Non-Syndromic Obesity +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LEP-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | LEP-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition | |
| | | Single nucleotide variant (missense variant) | LEP-related condition | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | 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) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (missense variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition | |
| | | Single nucleotide variant (missense variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Leptin dysfunction | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (missense variant) | LEP-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | LEP-related condition | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (frameshift variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (missense variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (synonymous variant) | LEP-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | LEP-related condition | |
| | | Single nucleotide variant (3 prime UTR variant) | LEP-related condition | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to congenital leptin deficiency +1 more | |