| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FAM216A, LOC130008745 (G12S) | Single nucleotide variant (missense variant) | not specified | |
| | FAM216A, LOC130008745 (G20V) | Single nucleotide variant (missense variant) | not specified | |
| | FAM216A, LOC130008745 (A38G) | Single nucleotide variant (missense variant) | not specified | |
| | FAM216A, LOC130008745 (T42I) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene