| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | FGD4-related disorder | |
| | | Single nucleotide variant (synonymous variant +3 more) | Charcot-Marie-Tooth disease type 4H +5 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene