| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130001386, DGAT1 (S18C) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | DGAT1, LOC130001386 (S14A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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