| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Heterotaxy, visceral, 5, autosomal | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Indel (inframe_indel) | Heterotaxy, visceral, 5, autosomal +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +2 more) | Heterotaxy, visceral, 5, autosomal | GConflicting classifications of pathogenicity |
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