| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FAM161A, LOC129933843 (E47Q) | Single nucleotide variant (missense variant +1 more) | Retinal dystrophy +2 more | |
| | FAM161A, LOC129933843 (A41V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | FAM161A, LOC129933843 (L39V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene