| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCNC3, LOC111811967 (Q41H) | Single nucleotide variant (5 prime UTR variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene