Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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 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: 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 GWASCAT 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: rs7711337
rs7711337
LOC105377698
0.800 GeneticVariation GWASDB 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: 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
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: rs4773054
rs4773054 		0.700 GeneticVariation GWASCAT A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? 25534755

2015
dbSNP: rs786205133
rs786205133
RLIM
C 0.700 GeneticVariation CLINVAR Syndromic X-linked intellectual disability segregating with a missense variant in RLIM. 25735484

2015
dbSNP: rs10858047
rs10858047 		T 0.700 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014