rs10038113
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs10058083
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs1006737
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Haplotype analyses showed that two haplotypes constructed from rs1006737 and rs4765905 were significantly associated with autism (p=0.030, 0.023, respectively; Global p=0.046).
|
26204268 |
2015 |
rs10185592
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs10205350
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs10239799
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale.
|
22935194 |
2013 |
rs10489525
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs10489525
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs10498676
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The A/A genotype of rs10498676 was correlated with a decline in the Autism Diagnostic Interview-Revised communication (verbal and nonverbal) domain.
|
30180836 |
2018 |
rs10500171
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The results show that a common noncoding variant (rs10500171) is associated with the increased risk for autism, and haplotype T-A (rs7794745- rs10500171, P=0.011) and haplotype A-T-A (rs10244837- rs7794745- rs10500171, P=0.032) also showed evidence of association.
|
20414140 |
2010 |
rs10513025
|
|
|
0.800 |
GeneticVariation |
GWASDB |
A genome-wide linkage and association scan reveals novel loci for autism.
|
19812673 |
2009 |
rs10513025
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
A genome-wide linkage and association scan reveals novel loci for autism.
|
19812673 |
2009 |
rs1051312
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We analysed five SNAP-25 gene polymorphisms (rs363050, rs363039, rs363043, rs3746544 and rs1051312) in 46 autistic children trying to correlate them with Childhood Autism Rating Scale and electroencephalogram (EEG) abnormalities.
|
25629685 |
2015 |
rs1053972
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We tested the hypothesis that the PCSK6 VNTR polymorphism rs1053972 influences the expression of handedness and aspects of dimensional schizotypy and autism.
|
26921480 |
2016 |
rs1057518345
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057518658
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057518993
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1057518999
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1057519440
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1057521223
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1060499733
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1060826
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The behavioral subdomain score of failure to use nonverbal behaviors to regulate social interaction in Autism Diagnostic Interview-Revised (ADI-R) was significantly higher in subjects with the GG or AG allele in rs1060826 of NOS-IIA compared to those who had the AA allele (P = 0.027).
|
18563708 |
2009 |
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome.
|
22595938 |
2012 |
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Lifetime cancer risks in individuals with germline PTEN mutations.
|
22252256 |
2012 |
rs1064794245
|
|
|
0.010 |
GeneticVariation |
BEFREE |
An Australian patient with autism was found to be heterozygous for two mutations in the gene encoding adenylosuccinate lyase (ASL), resulting in the protein mutations E80D and D87E.
|
15471876 |
2004 |