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 |
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 |
GWASDB |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
rs10489525
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |
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 |
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 |
|
|
|
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 |
rs1064794254
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism.
|
19238151 |
2010 |
rs1064794254
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay.
|
22609145 |
2012 |
rs1064794254
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
|
17704778 |
2007 |
rs10749886
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Individual common variants exert weak effects on the risk for autism spectrum disorders.
|
22843504 |
2012 |
rs1085307845
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1085307993
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs10858047
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Common genetic variants on 1p13.2 associate with risk of autism.
|
24189344 |
2014 |