| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129994388, TRIM36 (G20D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129994388, TRIM36 (I17T) | Single nucleotide variant (missense variant +1 more) | not specified | |
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