| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007282, SPSB2 (L88Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007282, SPSB2 (D76E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007282, SPSB2 (K51E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007282, SPSB2 (G47S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007282, SPSB2 (G41W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130007282, SPSB2 (P38S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene