Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2710102
rs2710102
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.030 GeneticVariation BEFREE In the updated meta-analysis, the association between the two frequently reported SNPs (rs2710102 and rs7794745) in CNTNAP2 and the risk of ASD was explored. 30681286 2019
dbSNP: rs2710102
rs2710102
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.030 GeneticVariation BEFREE We analyzed the SNPs (rs7794745 and rs2710102) in the CNTNAP2 gene of 210 individuals with idiopathic ASD and 200 non-autistic individuals by polymerase chain reaction-restriction fragment length polymorphism. 26909962 2016
dbSNP: rs2710102
rs2710102
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
CUI: C1510586
Disease:
Autism Spectrum Disorders
0.030 GeneticVariation BEFREE Although association was found with rs2710102, the risk allele (a) for the traits studied here is the nonrisk allele for ASD and specific language impairment. 21193173 2011