| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CCDC157, LOC130067209
+1 more (T17M) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CCDC157, LOC130067209
+1 more (P13L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CCDC157, LOC130067209
+1 more (P10L) | Single nucleotide variant (missense variant +1 more) | not specified | |
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