Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3827735
rs3827735
TRIM33
C 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs3827735
rs3827735
TRIM33
C 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs6537825
rs6537825
TRIM33
A 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs6537825
rs6537825
TRIM33
A 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs6661053
rs6661053
TRIM33
T 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs6661053
rs6661053
TRIM33
T 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs7511633
rs7511633
TRIM33
G 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs7511633
rs7511633
TRIM33
G 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs8453
rs8453
NRAS ; CSDE1
G 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs8453
rs8453
NRAS ; CSDE1
G 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs926938
rs926938
AMPD1
A 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs926938
rs926938
AMPD1
A 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs4150167
rs4150167
TAF1C
0.800 GeneticVariation GWASCAT Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs4150167
rs4150167
TAF1C
0.800 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs4675502
rs4675502
PARD3B
0.800 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs4675502
rs4675502
PARD3B
0.800 GeneticVariation GWASCAT Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs7711337
rs7711337
LOC105377698
0.800 GeneticVariation GWASCAT Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs7711337
rs7711337
LOC105377698
0.800 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs7834018
rs7834018 		0.800 GeneticVariation GWASCAT Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs7834018
rs7834018 		0.800 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs10513025
rs10513025 		0.800 GeneticVariation GWASDB A genome-wide linkage and association scan reveals novel loci for autism. 19812673

2009
dbSNP: rs10513025
rs10513025 		0.800 GeneticVariation GWASCAT A genome-wide linkage and association scan reveals novel loci for autism. 19812673

2009
dbSNP: rs1135402760
rs1135402760
BRSK2
C 0.700 GeneticVariation CLINVAR Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. 30879638

2019
dbSNP: rs1555453538
rs1555453538
POLG ; MIR6766
C 0.700 GeneticVariation CLINVAR Understanding the Epilepsy in POLG Related Disease. 28837072

2017
dbSNP: rs1566446604
rs1566446604
CHD8
G 0.700 CausalMutation CLINVAR A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review. 26789910

2016