| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion | Bethlem myopathy 1A | |
| | | Copy number loss | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806575, PER2 (N1248D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806575, PER2 (I1227T) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | not specified | |
| | | Copy number loss | not specified | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Deletion (inframe deletion) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (missense variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (intron variant) | PER2-related disorder | |
| | | Single nucleotide variant (missense variant) | PER2-related disorder | |
| | | Single nucleotide variant (missense variant) | PER2-related disorder | |
| | | Single nucleotide variant (missense variant) | PER2-related disorder | |
| | LOC126806575, PER2 (S1236L) | Single nucleotide variant (missense variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (intron variant) | PER2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | PER2-related disorder | |
| | | Single nucleotide variant (intron variant) | PER2-related disorder | |
| | | Single nucleotide variant (intron variant) | PER2-related disorder | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Duplication | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | PER2-related disorder +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | PER2-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC126806575, PER2 (R1250G) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (splice donor variant) | Advanced sleep phase syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Advanced sleep phase syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Advanced sleep phase syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Advanced sleep phase syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Advanced sleep phase syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Autism spectrum disorder | |
| | | Single nucleotide variant (missense variant) | Autism spectrum disorder | |
| | | Deletion | Bethlem myopathy 1A | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |