| | | Copy number gain | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | FZD6-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | FZD6-related condition | |
| | | Single nucleotide variant (intron variant) | FZD6-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | FZD6-related condition | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | FZD6-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | FZD6-related condition | |
| | | Single nucleotide variant (missense variant +3 more) | FZD6-related condition | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ANKRD46, ATP6V1C1 +40 more | Duplication | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Polydactyly | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not specified | |
| | DCAF4L2, DCSTAMP +333 more | Copy number gain | not specified | |
| | | Duplication | Cohen syndrome | |
| | | Single nucleotide variant (missense variant +3 more) | Nonsyndromic congenital nail disorder 1 | |
| | | Single nucleotide variant (splice acceptor variant) | Nonsyndromic congenital nail disorder 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Nonsyndromic congenital nail disorder 1 | |
| | | Single nucleotide variant (nonsense) | Nonsyndromic congenital nail disorder 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Nonsyndromic congenital nail disorder 1 | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | FZD6, LOC105369147 +2 more | Deletion | Primary amenorrhea | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Copy number gain | See cases | |
| | PPP1R16A, PPP1R42 +593 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (nonsense +2 more) | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant +2 more) | Nonsyndromic congenital nail disorder 1 +1 more | GConflicting classifications of pathogenicity |
| | LOC130001282, LOC130001283 +1552 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001328, LOC130001329 +1067 more | Copy number gain | See cases | |
| | LOC130000867, LOC130000868 +1686 more | Copy number gain | See cases | |
| | GPAT4, GPAT4-AS1 +3106 more | Copy number gain | See cases | |
| | LOC130000015, LOC130000016 +3658 more | Copy number gain | See cases | |
| | LOC129390031, LOC129390032 +234 more | Copy number loss | See cases | |
| | LOC130001243, LOC130001244 +1204 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130000897, LOC130000898 +1960 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130000067, LOC130000068 +3656 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC130000908, LOC130000909 +1406 more | Copy number gain | See cases | |
| | LOC130000899, LOC130000900 +154 more | Copy number loss | See cases | |
| | LOC110121192, LOC110121196 +3656 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant) | Nonsyndromic congenital nail disorder 1 +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Nonsyndromic congenital nail disorder 1 +1 more | |