Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83593
Gene Symbol: RASSF5
RASSF5
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 5091
Gene Symbol: PC
PC
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 92737
Gene Symbol: DNER
DNER
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 117583
Gene Symbol: PARD3B
PARD3B
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 54901
Gene Symbol: CDKAL1
CDKAL1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 55356
Gene Symbol: SLC22A15
SLC22A15
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 65217
Gene Symbol: PCDH15
PCDH15
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 152485
Gene Symbol: ZNF827
ZNF827
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 7704
Gene Symbol: ZBTB16
ZBTB16
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 221935
Gene Symbol: SDK1
SDK1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194

2013
Entrez Id: 51059
Gene Symbol: FAM135B
FAM135B
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194

2013
Entrez Id: 4745
Gene Symbol: NELL1
NELL1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194

2013
Entrez Id: 2241
Gene Symbol: FER
FER
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. 22935194

2013
Entrez Id: 7812
Gene Symbol: CSDE1
CSDE1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.420 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
Entrez Id: 51592
Gene Symbol: TRIM33
TRIM33
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.110 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
Entrez Id: 643586
Gene Symbol: PKMP1
PKMP1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014