| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129996825, RRAGD (K379N) | 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 | |
| | LOC129996831, RRAGD (G45C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996831, RRAGD (D36G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996831, RRAGD (G34V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996831, RRAGD (L28P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996831, RRAGD (D23E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129996831, RRAGD (E13K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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