| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FANCM, LOC130055524 (R18Q) | Single nucleotide variant (missense variant) | Spermatogenic failure 28 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spermatogenic failure 28 +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Spermatogenic failure 28 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (nonsense) | Premature ovarian failure 15 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Spermatogenic failure 28 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spermatogenic failure 28 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Spermatogenic failure 28 +4 more | GConflicting classifications of pathogenicity |
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