| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | B3GNT9, LOC130059177 (G31R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | B3GNT9, LOC130059177 (G31S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | B3GNT9, LOC130059177 (R6C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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