Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1614887
rs1614887
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
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: rs1796518
rs1796518
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0021704
Disease:
Intelligence 		T 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: rs1614887
rs1614887
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
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: rs1796518
rs1796518
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
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: rs2072806
rs2072806
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0018681
Disease:
Headache 		G 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773). 29397368 2018
dbSNP: rs2237234
rs2237234
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0036341
Disease:
Schizophrenia 		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: rs2237234
rs2237234
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		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: rs7756881
rs7756881
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053 2012
dbSNP: rs9461249
rs9461249
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053 2012
dbSNP: rs2072803
rs2072803
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASDB Common variants on chromosome 6p22.1 are associated with schizophrenia. 19571809 2009
dbSNP: rs2072806
rs2072806
Entrez Id: 10385
Gene Symbol: BTN2A2
BTN2A2
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASDB Common variants on chromosome 6p22.1 are associated with schizophrenia. 19571809 2009