| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CHD1L, LOC126805854 (A518S +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CHD1L, LOC126805854 (R706H +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CHD1L, LOC126805854 (A746T +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CHD1L, LOC126805854 (A537V +7 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
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