| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CDAN1, LOC130056931 (T165M) | Single nucleotide variant (missense variant) | Anemia, congenital dyserythropoietic, type 1a +1 more | |
| | CDAN1, LOC130056931 (G149E) | Single nucleotide variant (missense variant) | not provided | |
| | CDAN1, LOC130056931 (A148T) | Single nucleotide variant (missense variant) | not provided | |
| | CDAN1, LOC130056931 (A96V) | Single nucleotide variant (missense variant) | not provided | |
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