Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906943
rs387906943
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C1970200
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12
0.800 GeneticVariation UNIPROT ST3GAL3 mutations impair the development of higher cognitive functions. 21907012 2011
dbSNP: rs387906943
rs387906943
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C1970200
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12
A 0.800 CausalMutation CLINVAR
dbSNP: rs12410444
rs12410444
Entrez Id: 6487;101929592
Gene Symbol: ST3GAL3;LOC101929592
ST3GAL3;LOC101929592
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs12410444
rs12410444
Entrez Id: 6487;101929592
Gene Symbol: ST3GAL3;LOC101929592
ST3GAL3;LOC101929592
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs2486012
rs2486012
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs4660261
rs4660261
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs56319043
rs56319043
Entrez Id: 6487;9682;100132774
Gene Symbol: ST3GAL3;KDM4A;KDM4A-AS1
ST3GAL3;KDM4A;KDM4A-AS1
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
C 0.700 GeneticVariation GWASCAT Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality. 30610198 2019
dbSNP: rs56319043
rs56319043
Entrez Id: 6487;9682;100132774
Gene Symbol: ST3GAL3;KDM4A;KDM4A-AS1
ST3GAL3;KDM4A;KDM4A-AS1
CUI: C3160814
Disease:
Cannabis use
C 0.700 GeneticVariation GWASCAT Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality. 30610198 2019
dbSNP: rs6429637
rs6429637
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs6674176
rs6674176
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs112984125
rs112984125
Entrez Id: 6487;100132774
Gene Symbol: ST3GAL3;KDM4A-AS1
ST3GAL3;KDM4A-AS1
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
A 0.700 GeneticVariation GWASCAT A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. 29325848 2018
dbSNP: rs11577684
rs11577684
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
C 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs246776
rs246776
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs2906455
rs2906455
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs4660749
rs4660749
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs6656457
rs6656457
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
C 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs12040333
rs12040333
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444 2017
dbSNP: rs12040333
rs12040333
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C1611184
Disease:
Calcification of coronary artery
0.700 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444 2017
dbSNP: rs6674176
rs6674176
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694 2017
dbSNP: rs3011225
rs3011225
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
G 0.700 GeneticVariation GWASCAT Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728 2013
dbSNP: rs11210927
rs11210927
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12122504
rs12122504
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs12133508
rs12133508
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs6701645
rs6701645
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs1557612719
rs1557612719
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
CUI: C1970200
Disease:
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12
T 0.700 CausalMutation CLINVAR