Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10513025
rs10513025
0.810 GeneticVariation BEFREE We have genotyped 746 individuals from 227 families of the Italian Autism Network using allelic discrimination TaqMan assays for seven common single-nucleotide polymorphisms: rs2292813 (SLC25A12 gene), rs35678 (ATP2B2 gene), rs4307059 (between CDH9 and CDH10 genes), rs10513025 (between SEMA5A and TAS2R1 genes), rs6872664 (PITX1 gene), rs1861972 (EN2 gene), and rs4141463 (MACROD2 gene). 22739633

2012

dbSNP: rs4141463
rs4141463
0.810 GeneticVariation BEFREE Therefore, this study does not provide support for the reported association between rs4141463 and autism. 21656903

2012

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

2011

dbSNP: rs4141463
rs4141463
0.810 GeneticVariation GWASCAT A genome-wide scan for common alleles affecting risk for autism. 20663923

2011

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

2009

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

2009

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

2015

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

2015

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

2015

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

2015

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

2013

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

2013

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

2013

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

2013

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

2013

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

2013

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

2013

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

2013

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

2009

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

2009

dbSNP: rs1877455
rs1877455
0.710 GeneticVariation BEFREE 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

2015

dbSNP: rs1877455
rs1877455
0.710 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2015

dbSNP: rs10489525
rs10489525
0.700 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2015

dbSNP: rs11102800
rs11102800
0.700 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2015

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

2015