| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARMC5, LOC130058906 (G97S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ARMC5, LOC130058906 (A112V +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ARMC5, LOC130058906 (A129T +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ARMC5, LOC130058906 (L131W +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ARMC5, LOC130058906 (C145S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene