| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FCMR, LOC126805991 (M220I +8 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FCMR, LOC126805991 (A216T +8 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene