| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KIF7, LOC126862216 (T1109M) | Single nucleotide variant (missense variant) | Hydrolethalus syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | Male infertility due to gonadal dysgenesis or sperm disorder +8 more | GConflicting classifications of pathogenicity |
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