| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130063760, SAMD1 (A22T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063760, SAMD1 (S28Y) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063760, SAMD1 (P29L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063760, SAMD1 (E33D) | Single nucleotide variant (missense variant) | not specified | |
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