Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1718101
rs1718101
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
CUI: C0004352
Disease:
Autistic Disorder
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504 2012