| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130000540, VCPIP1 (A167V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130000540, VCPIP1 (D51E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130000540, VCPIP1 (G34R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130000540, VCPIP1 (P16S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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