Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13195401
rs13195401
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs1977199
rs1977199
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		A 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: rs1977199
rs1977199
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
CUI: C0036341
Disease:
Schizophrenia 		A 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: rs1977200
rs1977200
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
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: rs2273558
rs2273558
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
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: rs2273558
rs2273558
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
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: rs3734542
rs3734542
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
CUI: C0684249
Disease:
Carcinoma of lung 		A 0.700 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730 2017
dbSNP: rs3799380
rs3799380
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
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: rs7763910
rs7763910
Entrez Id: 11120;285819
Gene Symbol: BTN2A1;LOC285819
BTN2A1;LOC285819
CUI: C0017168
Disease:
Gastroesophageal reflux disease 		G 0.700 GeneticVariation GWASCAT Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. 31527586 2019
dbSNP: rs6929846
rs6929846
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
CUI: C0027051
Disease:
Myocardial Infarction 		0.780 GeneticVariation GWASDB The rs6929846 SNP of BTN2A1, but not rs2569512 of ILF3, was also significantly associated with MI in Japanese subject panel C. However, the association of neither rs6929846 nor rs2569512 with MI was replicated in the Korean population. 21211798 2011
dbSNP: rs13195509
rs13195509
Entrez Id: 11120
Gene Symbol: BTN2A1
BTN2A1
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		A 0.700 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463 2014