Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4141463
rs4141463
MACROD2
0.820 GeneticVariation GWASCAT A genome-wide scan for common alleles affecting risk for autism. 20663923

2010
dbSNP: rs4141463
rs4141463
MACROD2
0.820 GeneticVariation GWASDB A genome-wide scan for common alleles affecting risk for autism. 20663923

2010
dbSNP: rs1877455
rs1877455 		A 0.810 GeneticVariation GWASDB Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism. 24189344

2014
dbSNP: rs1877455
rs1877455 		T 0.810 GeneticVariation GWASDB Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism. 24189344

2014
dbSNP: rs1877455
rs1877455 		T 0.810 GeneticVariation GWASCAT Meta-analysis identified three single-nucleotide polymorphisms, rs936938 (P=4.49 × 10(-8)), non-synonymous rs6537835 (P=3.26 × 10(-8)) and rs1877455 (P=8.70 × 10(-8)), and related haplotypes, AMPD1-NRAS-CSDE1, TRIM33 and TRIM33-BCAS2, associated with autism; all were mapped to a previously reported linkage region (1p13.2) with autism. 24189344

2014
dbSNP: rs4307059
rs4307059 		T 0.810 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs4307059
rs4307059 		T 0.810 GeneticVariation GWASCAT Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs10489525
rs10489525
CSDE1
G 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014
dbSNP: rs10489525
rs10489525
CSDE1
G 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

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

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

2014