| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCNN2, LOC101927078 (L677I +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KCNN2, LOC101927078 (K659R +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KCNN2, LOC101927078 (M756R +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KCNN2, LOC101927078 (S210P +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | KCNN2, LOC101927078 (R211Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene