| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130061738, ST6GALNAC2 (G21V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061738, ST6GALNAC2 (C19F) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061738, ST6GALNAC2 (L15P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130061738, ST6GALNAC2 (L12M) | Single nucleotide variant (missense variant) | not specified | |
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