| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056842 (R741P) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056842 (G737S) | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056841 (A15T) | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056842 (A751S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056842 (T731M) | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056842 (E752A) | Single nucleotide variant (missense variant) | not specified | |
| | DISP2, LOC130056842 (V739I) | Single nucleotide variant (missense variant) | not specified | |
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