| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FBXL6, LOC130001388 (K80T) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (P68L) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (R56W) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (R65C) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (R14W) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (G84R) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (Y37C) | Single nucleotide variant (missense variant) | not specified | |
| | FBXL6, LOC130001388 (G53S) | Single nucleotide variant (missense variant) | not provided | |
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