| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FOXD2, LOC129930497 (S13C) | Single nucleotide variant (missense variant) | not specified | |
| | FOXD2, LOC129930497 (G33C) | Single nucleotide variant (missense variant) | not specified | |
| | FOXD2, LOC129930497 (G36R) | Single nucleotide variant (missense variant) | not specified | |
| | FOXD2, LOC129930497 (R42C) | Single nucleotide variant (missense variant) | not specified | |
| | FOXD2, LOC129930497 (R42H) | Single nucleotide variant (missense variant) | not specified | |
| | FOXD2, LOC129930497 (R46C) | Single nucleotide variant (missense variant) | not specified | |
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