rs1396313317
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.
|
30763456 |
2019 |
rs7794745
|
|
|
0.040 |
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 |
rs7794745
|
|
|
0.040 |
GeneticVariation |
BEFREE |
The results revealed higher frequency distributions statistically significant (P = 0.034) of the homozygous SNP rs7794745 (presumed risk genotype) in ASD patients as compared with control subjects.
|
26909962 |
2016 |
rs7794745
|
|
|
0.040 |
GeneticVariation |
BEFREE |
Five single nucleotide polymorphisms in CNTNAP2 (including rs7794745 and rs2710102, previously associated with ASDs) were genotyped.
|
21193173 |
2011 |
rs7794745
|
|
|
0.040 |
GeneticVariation |
BEFREE |
A total of 110 adult patients with ASD (n=61) or ADHD (n=49) with or without a lifetime history of SUD participated in a study in which we genotyped polymorphisms in five known candidate genes for (one of) the disorders, i.e. the 5HTTLPR in SLC6A4/5-HTT, rs1800497 (TaqIA C>T) in DRD2, rs7794745 in CNTNAP2, rs1843809 in TPH2, and rs6565113 in CDH13.
|
20446882 |
2010 |
rs2710102
|
|
|
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 |
rs2710102
|
|
|
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 |
rs2710102
|
|
|
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 |
rs121908445
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Then, we show that the two ASD variants I869T and G731S, which present impaired binding to Contactin2/TAG-1, do not rescue axonal growth deficits.
|
29788201 |
2018 |
rs369867547
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Then, we show that the two ASD variants I869T and G731S, which present impaired binding to Contactin2/TAG-1, do not rescue axonal growth deficits.
|
29788201 |
2018 |