Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10038113
rs10038113 		0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs10058083
rs10058083 		0.700 GeneticVariation GWASDB Common genetic variants on 5p14.1 associate with autism spectrum disorders. 19404256

2009
dbSNP: rs1006737
rs1006737
CACNA1C
0.010 GeneticVariation BEFREE Haplotype analyses showed that two haplotypes constructed from rs1006737 and rs4765905 were significantly associated with autism (p=0.030, 0.023, respectively; Global p=0.046). 26204268

2015
dbSNP: rs10185592
rs10185592
LOC105373847
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs10205350
rs10205350
GALNT14
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012
dbSNP: rs10239799
rs10239799 		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: rs10489525
rs10489525
CSDE1
G 0.800 GeneticVariation GWASCAT Common genetic variants on 1p13.2 associate with risk of autism. 24189344

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

2014
dbSNP: rs10498676
rs10498676
ELOVL2
0.010 GeneticVariation BEFREE The A/A genotype of rs10498676 was correlated with a decline in the Autism Diagnostic Interview-Revised communication (verbal and nonverbal) domain. 30180836

2018
dbSNP: rs10500171
rs10500171
CNTNAP2
0.010 GeneticVariation BEFREE The results show that a common noncoding variant (rs10500171) is associated with the increased risk for autism, and haplotype T-A (rs7794745- rs10500171, P=0.011) and haplotype A-T-A (rs10244837- rs7794745- rs10500171, P=0.032) also showed evidence of association. 20414140

2010
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: rs1051312
rs1051312
SNAP25 ; SNAP25-AS1
0.010 GeneticVariation BEFREE We analysed five SNAP-25 gene polymorphisms (rs363050, rs363039, rs363043, rs3746544 and rs1051312) in 46 autistic children trying to correlate them with Childhood Autism Rating Scale and electroencephalogram (EEG) abnormalities. 25629685

2015
dbSNP: rs1053972
rs1053972
KLK3
0.010 GeneticVariation BEFREE We tested the hypothesis that the PCSK6 VNTR polymorphism rs1053972 influences the expression of handedness and aspects of dimensional schizotypy and autism. 26921480

2016
dbSNP: rs1057518345
rs1057518345
ADNP
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518658
rs1057518658
SCN2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518993
rs1057518993
IQSEC2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518999
rs1057518999
FOXP1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519440
rs1057519440
GSPT2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057521223
rs1057521223
SCN2A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499733
rs1060499733
DHX30
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060826
rs1060826
NOS2
0.010 GeneticVariation BEFREE The behavioral subdomain score of failure to use nonverbal behaviors to regulate social interaction in Autism Diagnostic Interview-Revised (ADI-R) was significantly higher in subjects with the GG or AG allele in rs1060826 of NOS-IIA compared to those who had the AA allele (P = 0.027). 18563708

2009
dbSNP: rs1064793345
rs1064793345
PTEN
C 0.700 GeneticVariation CLINVAR Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome. 22595938

2012
dbSNP: rs1064793345
rs1064793345
PTEN
C 0.700 GeneticVariation CLINVAR Lifetime cancer risks in individuals with germline PTEN mutations. 22252256

2012
dbSNP: rs1064794245
rs1064794245
ADSL
0.010 GeneticVariation BEFREE An Australian patient with autism was found to be heterozygous for two mutations in the gene encoding adenylosuccinate lyase (ASL), resulting in the protein mutations E80D and D87E. 15471876

2004