| | LOC129388541, LOC129388542 +570 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC132088736, LOC132088737 +557 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC126805749, LOC126805750 +331 more | Copy number loss | See cases | |
| | LOC129930732, LOC129930733 +269 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (5 prime UTR variant) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (5 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | LEPR, LEPROT (V17M +1 more) | Single nucleotide variant (5 prime UTR variant +1 more) | not specified | |
| | LEPR, LEPROT (L21R +1 more) | Single nucleotide variant (5 prime UTR variant +1 more) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | LEPR, LEPROT (V41I +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LEPR, LEPROT (R76W +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LEPR, LEPROT (I77T +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (synonymous variant) | LEPR-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Insertion (intron variant) | not provided | |
| | | Microsatellite (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder | |
| | | Single nucleotide variant (synonymous variant) | LEPR-related disorder +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (synonymous variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | LEPR-related disorder | |
| | | Single nucleotide variant (intron variant) | Obesity due to leptin receptor gene deficiency +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (intron variant) | LEPR-related disorder | |
| | | Deletion (intron variant) | LEPR-related disorder | |
| | | Deletion (intron variant) | LEPR-related disorder | |
| | | Deletion (intron variant) | LEPR-related disorder | |
| | | Deletion (intron variant) | LEPR-related disorder | |
| | | Insertion (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 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | LEPR-related disorder | |
| | | Insertion (intron variant) | not provided | |
| | | Insertion (splice acceptor variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Obesity due to leptin receptor gene deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Obesity due to leptin receptor gene deficiency | |
| | | Duplication (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | LEPR-related disorder | |
| | | Single nucleotide variant (synonymous variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 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 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | LEPR-related disorder | |
| | | Single nucleotide variant (missense variant) | Monogenic diabetes +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to leptin receptor gene deficiency +1 more | |