| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CRELD2, LOC130067777 (S267L +3 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CRELD2, LOC130067777 (E274K +3 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CRELD2, LOC130067777 (Y287C +3 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
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