| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130007872, SMARCD1 (P37L) | Single nucleotide variant (missense variant) | not provided | |
| | LOC130007872, SMARCD1 (P44L) | Single nucleotide variant (missense variant) | not provided | |
| | LOC130007872, SMARCD1 (M53T) | Single nucleotide variant (missense variant) | not provided | |
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