| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CCDC169-SOHLH2, SOHLH2 (R402Q +1 more) | Single nucleotide variant (missense variant) | CCDC169-SOHLH2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | CCDC169-SOHLH2-related disorder | |
| | | Single nucleotide variant (synonymous variant) | CCDC169-SOHLH2-related disorder | |
| | | Single nucleotide variant (intron variant) | CCDC169-SOHLH2-related disorder | |
| | CCDC169-SOHLH2, SOHLH2 (T112I +1 more) | Single nucleotide variant (missense variant) | CCDC169-SOHLH2-related disorder | |
Click to view in NCBI Gene