| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC124416837, PLA2G12B (C186Y +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC124416837, PLA2G12B (T170A +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC124416837, PLA2G12B (V168M +2 more) | Single nucleotide variant (missense variant) | not specified | |
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