Source: CURATED ×
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: rs10185592
rs10185592
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012

dbSNP: rs10205350
rs10205350
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
G 0.800 GeneticVariation GWASDB Common genetic variants on 1p13.2 associate with risk of autism. 24189344

2014

dbSNP: rs10489525
rs10489525
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: rs1057518345
rs1057518345
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518658
rs1057518658
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518993
rs1057518993
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518999
rs1057518999
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519440
rs1057519440
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057521223
rs1057521223
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499733
rs1060499733
G 0.700 GeneticVariation CLINVAR

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

2012

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

2012

dbSNP: rs1064794254
rs1064794254
C 0.700 CausalMutation CLINVAR Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism. 19238151

2010

dbSNP: rs1064794254
rs1064794254
C 0.700 CausalMutation CLINVAR Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay. 22609145

2012

dbSNP: rs1064794254
rs1064794254
C 0.700 CausalMutation CLINVAR Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation. 17704778

2007

dbSNP: rs10749886
rs10749886
0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504

2012

dbSNP: rs1085307845
rs1085307845
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
T 0.700 GeneticVariation CLINVAR

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

2014