| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | CLPTM1-related disorder | |
| | CLPTM1, LOC130064657 (G20D) | Single nucleotide variant (missense variant +1 more) | not specified +1 more | |
Click to view in NCBI Gene