| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | C1QTNF1, LOC126862658 (S143G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862658, C1QTNF1 (R22G +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (Y79C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (P190R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (R22H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (T43I +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (L174V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (T164M +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (A4P +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | C1QTNF1, LOC126862658 (A88T +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
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