Links from PubMed
Items: 3
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Microsatellite (frameshift variant) | Fanconi anemia complementation group N +5 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant) | Hereditary breast ovarian cancer syndrome +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene