| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | RAB39B-related condition +4 more | |
| | | Single nucleotide variant (synonymous variant) | RAB39B-related condition +2 more | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene