Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13218591
rs13218591
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C1269683
Disease:
Major Depressive Disorder 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs2073526
rs2073526
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C0596887
Disease:
mathematical ability 		G 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs2073526
rs2073526
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs9379870
rs9379870
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs13218591
rs13218591
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs13218591
rs13218591
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		T 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs9348712
rs9348712
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs9379855
rs9379855
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs9379857
rs9379857
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs9104
rs9104
Entrez Id: 11118
Gene Symbol: BTN3A2
BTN3A2
CUI: C0019196
Disease:
Hepatitis C 		0.010 GeneticVariation BEFREE BTN3A2 rs9104 was strongly associated with genotype 1 infection and the haplotype BTN3A3 rs13220495 CC+IL28B genotype CC was universal in patients with hepatitis C genotype 3a. 25928882 2016