| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CIAO2B, LOC130059167 (P56R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CIAO2B, LOC130059168 (P38L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CIAO2B, LOC130059168 (E33G) | Single nucleotide variant (missense variant +1 more) | not specified | |
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