| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CNTNAP2, LOC126860216 (E982G) | Single nucleotide variant (missense variant) | Autism, susceptibility to, 15 +2 more | |
| | CNTNAP2, LOC126860216 (H985Q) | Single nucleotide variant (missense variant) | Autism, susceptibility to, 15 +2 more | |
Click to view in NCBI Gene