| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KLHDC9, LOC129931749 (P19L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHDC9, LOC129931749 (A29V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLHDC9, LOC129931749 (L47V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KLHDC9, LOC129931750 (R79L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KLHDC9, LOC129931750 (G75C) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene