| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | AFG2B, LOC130056998 (G203R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | AFG2B, LOC130056998 (E207G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | AFG2B, LOC130056998 (A225V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | AFG2B, LOC130056998 (T227P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene