| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CXADR, BTG3 (P277L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BTG3, CXADR (F179I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BTG3, CXADR (V164A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BTG3, CXADR (S207L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | BTG3, CXADR (S116T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene