| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DOCK6, DOCK6-AS1 (V1435M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | DOCK6, DOCK6-AS1 (R1338* +1 more) | Single nucleotide variant (nonsense) | Adams-Oliver syndrome 2 +1 more | GPathogenic/Likely pathogenic |
| | DOCK6, DOCK6-AS1 (R1305C +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
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