| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +2 more) | AIFM1-related condition +7 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Charcot-Marie-Tooth Neuropathy X +2 more | |
| | LOC130068679, RAB33A
+1 more (P35S) | Single nucleotide variant (missense variant +1 more) | Charcot-Marie-Tooth disease X-linked recessive 4 +6 more | |
| | AIFM1, LOC130068679
+1 more | Single nucleotide variant (synonymous variant +1 more) | Charcot-Marie-Tooth Neuropathy X +4 more | |
Click to view in NCBI Gene