| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | CELSR1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | CELSR1-related disorder | |
| | CELSR1, LOC126863170 (T1362M) | Single nucleotide variant (missense variant) | CELSR1-related disorder | |
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