| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases | |
| | CNTNAP1, LOC125177481 (L46I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CNTNAP1, LOC125177481 (I58V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene