autistic disorder Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years. (Human Disease Ontology, DOID_12849)
External Link
Similar Terms
Downloads & Tools


10 genes associated with the disease autistic disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
SMOC1 SPARC related modular calcium binding 1 1.62029
LDAH lipid droplet associated hydrolase 1.29875
SOX7 SRY (sex determining region Y)-box 7 1.19999
GLIS1 GLIS family zinc finger 1 1.19762
SORBS2 sorbin and SH3 domain containing 2 1.18698
LIN28B lin-28 homolog B (C. elegans) 1.14463
NEDD4L neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase 1.03626
C2ORF91 chromosome 2 open reading frame 91 0.99494
ZNF695 zinc finger protein 695 0.984747
VAV3 vav 3 guanine nucleotide exchange factor 0.964504