| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FANCM, LOC130055524 (R18Q) | Single nucleotide variant (missense variant) | Fanconi anemia complementation group A +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +7 more | |
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