| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | GPC3-related disorder +4 more | |
| | | Duplication (intron variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Deletion (intron variant) | not specified +3 more | |
| | | Deletion (intron variant) | Wilms tumor 1 +5 more | |
Click to view in NCBI Gene