| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ARL6IP1, LOC130058582 (N10K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 61 | |
| | ARL6IP1, LOC130058582 (T9S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 61 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 61 | |
| | ARL6IP1, LOC130058582 (N6S) | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 61 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 61 | |
| | | Duplication (intron variant) | Hereditary spastic paraplegia 61 | |
| | ARL6IP1, LOC130058582 (N10S) | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 61 | |
| | ARL6IP1, LOC130058582 (T9S) | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 61 +1 more | |
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