| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HOXA13, LOC107126288 (S176N) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | HOXA13, LOC107126288 (A167S) | Single nucleotide variant (missense variant) | Guttmacher syndrome +2 more | |
| | HOXA13, LOC107126288 (P166T) | Single nucleotide variant (missense variant) | Guttmacher syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hand-foot-genital syndrome +2 more | |
| | | Deletion (inframe_deletion) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | not provided +2 more | |
| | HOXA13, LOC107126288 (R88H) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | HOXA13, LOC107126288 (P59S) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | HOXA13, LOC107126288 (V16I) | Single nucleotide variant (missense variant) | Guttmacher syndrome +2 more | |
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