| Asperger Syndrome |
C0236792 |
DISC1
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
17579608 |
- |
|
SLC6A4
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
18197083 |
- |
|
VIP
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
23849776 |
- |
| ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1 (disorder) |
C1845341 |
NLGN3
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
12669065 |
- |
| NON RARE IN EUROPE: Asperger syndrome |
1162 |
NLGN3
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
- |
- |
|
NLGN4X
|
Unknown
Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations
|
- |
- |