| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FAM117B, LOC129935439 (G84S) | Single nucleotide variant (missense variant) | not specified | |
| | FAM117B, LOC129935439 (R86H) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene