| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | ABL1-related congenital heart defects and skeletal malformations syndrome | |
| | ABL1, LOC107980440 (W48S +1 more) | Single nucleotide variant (missense variant) | Congenital heart defects and skeletal malformations syndrome | |
| | | Single nucleotide variant (missense variant) | Congenital heart defects and skeletal malformations syndrome +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Congenital heart defects and skeletal malformations syndrome +4 more | |
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