| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Inclusion Body Myopathy, Dominant +5 more | |
| | | Single nucleotide variant (missense variant) | FANCG-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Fanconi anemia complementation group G +5 more | |
| | | Single nucleotide variant (missense variant) | FANCG-related condition +6 more | |
Click to view in NCBI Gene