Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10904487
rs10904487 		0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs10942147
rs10942147
MSNP1
0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs11102800
rs11102800
TRIM33
C 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11102800
rs11102800
TRIM33
C 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11102807
rs11102807 		A 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11102807
rs11102807 		A 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11118968
rs11118968
RASSF5
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs11211996
rs11211996
GUCY1A2
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs1135402760
rs1135402760
BRSK2
C 0.700 GeneticVariation CLINVAR Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. 30879638

2019
dbSNP: rs113871094
rs113871094
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs113994098
rs113994098
POLG
T 0.700 CausalMutation CLINVAR Disease mutations in the human mitochondrial DNA polymerase thumb subdomain impart severe defects in mitochondrial DNA replication. 19478085

2009
dbSNP: rs113994098
rs113994098
POLG
T 0.700 CausalMutation CLINVAR Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia. 12210792

2002
dbSNP: rs113994098
rs113994098
POLG
T 0.700 CausalMutation CLINVAR Mitochondrial DNA polymerase gamma mutations: an ever expanding molecular and clinical spectrum. 21880868

2011
dbSNP: rs11582563
rs11582563
TRIM33
G 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11582563
rs11582563
TRIM33
G 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11585926
rs11585926
TRIM33
T 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11585926
rs11585926
TRIM33
T 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11587400
rs11587400
PKMP1
C 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11587400
rs11587400
PKMP1
C 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11589568
rs11589568
TRIM33
T 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11589568
rs11589568
TRIM33
T 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs11739167
rs11739167
MSNP1
0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs11899372
rs11899372 		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
dbSNP: rs121909323
rs121909323
CACNA1A
A 0.700 CausalMutation CLINVAR CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms. 25735478

2015
dbSNP: rs12194182
rs12194182
SLC22A3
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012