rs4307059
|
|
Autistic Disorder
|
T |
0.810 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs4307059
|
|
Autistic Disorder
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs1877455
|
|
Autistic Disorder
|
A |
0.810 |
GeneticVariation
|
GWASDB |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs1877455
|
|
Autistic Disorder
|
T |
0.810 |
GeneticVariation
|
GWASDB |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs1877455
|
|
Autistic Disorder
|
T |
0.810 |
GeneticVariation
|
GWASCAT |
Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism.
|
24189344 |
2014 |
rs7834018
|
|
Autistic Disorder
|
|
0.800 |
GeneticVariation
|
GWASCAT |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs7834018
|
|
Autistic Disorder
|
|
0.800 |
GeneticVariation
|
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs11102807
|
|
Autistic Disorder
|
A |
0.800 |
GeneticVariation
|
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs11102807
|
|
Autistic Disorder
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs10513025
|
|
Autistic Disorder
|
|
0.800 |
GeneticVariation
|
GWASDB |
A genome-wide linkage and association scan reveals novel loci for autism.
|
19812673 |
2009 |
rs10513025
|
|
Autistic Disorder
|
|
0.800 |
GeneticVariation
|
GWASCAT |
A genome-wide linkage and association scan reveals novel loci for autism.
|
19812673 |
2009 |
rs932026
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs922551
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs7800565
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs7705715
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs7704909
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs7380139
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs6894838
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs6894102
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs6891206
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs6873221
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs6452305
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs6452304
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
|
19404256 |
2009 |
rs519700
|
|
Autistic Disorder
|
|
0.700 |
GeneticVariation
|
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs4925506
|
|
Autistic Disorder
|
|
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 |