| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | SDCBP2, FKBP1A-SDCBP2 (S288P +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (H282Y +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (H186P +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (V173I +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (G152R +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | SDCBP2, FKBP1A-SDCBP2 (G140V +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (V131G +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (R106W +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (P103L +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (S80L +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (S80A +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (M54T) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | FKBP1A-SDCBP2, SDCBP2 (P40L) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
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