| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CHFR, LOC126861701 (V346M +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | CHFR, LOC126861701 (S238L +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | CHFR, LOC126861701 (I293S +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | CHFR, LOC126861701 (L346V +3 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
Click to view in NCBI Gene