| | LOC126806176, LOC126806177 +1047 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129933242, LOC129933243 +1631 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129934199, LOC129934200 +2457 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129933291, LOC129933292 +142 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | 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 condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | POMC-related condition | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | POMC-related condition | |
| | | 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 condition | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +3 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe deletion) | POMC-related condition | |
| | | Single nucleotide variant (synonymous variant) | Obesity +1 more | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +3 more | |
| | | Single nucleotide variant (missense variant) | Obesity due to pro-opiomelanocortin deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | POMC-related condition | |
| | | 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 condition | |
| | | 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 condition +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | POMC-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | POMC-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | POMC-related condition | |
| | | 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 +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Obesity due to pro-opiomelanocortin deficiency | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | POMC-related condition | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +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) | Obesity +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) | Obesity +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 condition | |
| | | 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) | not specified +3 more | |
| | | Insertion (inframe_indel) | not provided | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +1 more | |
| | | Microsatellite (inframe insertion) | POMC-related condition | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | POMC-related condition | |
| | | 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 condition +1 more | |
| | | Single nucleotide variant (missense variant) | POMC-related condition | |
| | | 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 condition | |
| | | Single nucleotide variant (missense variant) | POMC-related condition +1 more | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | POMC-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | POMC-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |