Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 55689
Gene Symbol: YEATS2
YEATS2
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: 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: 114795
Gene Symbol: TMEM132B
TMEM132B
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: 9013
Gene Symbol: TAF1C
TAF1C
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.400 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 23224
Gene Symbol: SYNE2
SYNE2
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: 114815
Gene Symbol: SORCS1
SORCS1
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: 101928079
Gene Symbol: SLC44A3-AS1
SLC44A3-AS1
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: 201266
Gene Symbol: SLC39A11
SLC39A11
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: 9962
Gene Symbol: SLC23A2
SLC23A2
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: 6581
Gene Symbol: SLC22A3
SLC22A3
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: 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: 9501
Gene Symbol: RPH3AL
RPH3AL
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: 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: 5879
Gene Symbol: RAC1
RAC1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.120 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
Entrez Id: 5493
Gene Symbol: PPL
PPL
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: 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
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: 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: 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: 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: 89795
Gene Symbol: NAV3
NAV3
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: 4479
Gene Symbol: MSNP1
MSNP1
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.100 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009