| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DOK7, LOC126806951 (V181I +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | |
| | DOK7, LOC126806951 (R184Q +2 more) | Single nucleotide variant (missense variant +1 more) | Fetal akinesia deformation sequence 1 +3 more | |
| | LOC126806951, DOK7 (E188D +2 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | DOK7, LOC126806951 (S193G +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +3 more | |
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