| | | Single nucleotide variant (3 prime UTR variant) | Obesity due to pro-opiomelanocortin deficiency +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Deletion (3 prime UTR variant) | Monogenic Non-Syndromic Obesity +1 more | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe deletion) | POMC-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Obesity +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to pro-opiomelanocortin deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Duplication (inframe_insertion) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Obesity due to pro-opiomelanocortin deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Obesity due to pro-opiomelanocortin deficiency +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Obesity +1 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to pro-opiomelanocortin deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Obesity +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Obesity due to pro-opiomelanocortin deficiency | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | Obesity due to pro-opiomelanocortin deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (nonsense) | Obesity due to pro-opiomelanocortin deficiency | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (frameshift variant) | Obesity due to pro-opiomelanocortin deficiency | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Obesity due to pro-opiomelanocortin deficiency | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | | Insertion (frameshift variant) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided +2 more | |
| | | Insertion | Obesity | |
| | | Microsatellite (inframe_insertion) | Monogenic Non-Syndromic Obesity +3 more | |
| | | Insertion (inframe_indel) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Microsatellite (inframe insertion) | POMC-related disorder | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Indel (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Obesity +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Obesity due to pro-opiomelanocortin deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder +1 more | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense 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) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (synonymous variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (missense variant) | POMC-related disorder | |
| | | Single nucleotide variant (nonsense) | Obesity due to pro-opiomelanocortin deficiency | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |