BSN, bassoon presynaptic cytomatrix protein, 8927

N. diseases: 20; N. variants: 23
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation BEFREE BSN and MST1 were significantly associated with either CD (P(rs9858542) 2.5 x 10(-7); P(rs3197999) 3.9 x 10(-7)), and UC (P(rs9858542) = 3.1 x 10(-4); P(rs3197999) = 8 x 10(-4)). 20024904 2010
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0009324
Disease:
Ulcerative Colitis 		0.810 GeneticVariation BEFREE BSN and MST1 were significantly associated with either CD (P(rs9858542) 2.5 x 10(-7); P(rs3197999) 3.9 x 10(-7)), and UC (P(rs9858542) = 3.1 x 10(-4); P(rs3197999) = 8 x 10(-4)). 20024904 2010
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0009324
Disease:
Ulcerative Colitis 		0.810 GeneticVariation GWASDB Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. 19915572 2009
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0009324
Disease:
Ulcerative Colitis 		0.810 GeneticVariation GWASCAT Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. 19915572 2009
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation GWASDB Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261 2007
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0010346
Disease:
Crohn Disease 		A 0.810 GeneticVariation GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300 2007
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0010346
Disease:
Crohn Disease 		A 0.810 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300 2007
dbSNP: rs9858542
rs9858542
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0010346
Disease:
Crohn Disease 		0.810 GeneticVariation GWASCAT Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. 17554261 2007
dbSNP: rs115548824
rs115548824
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13096480
rs13096480
Entrez Id: 8927
Gene Symbol: BSN
BSN
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: rs35999162
rs35999162
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C1314691
Disease:
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56116382
rs56116382
Entrez Id: 8927
Gene Symbol: BSN
BSN
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: rs56176327
rs56176327
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0021704
Disease:
Intelligence 		C 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: rs11130206
rs11130206
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0201657
Disease:
C-reactive protein measurement 		C 0.700 GeneticVariation GWASCAT Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. 30388399 2018
dbSNP: rs11917431
rs11917431
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0596887
Disease:
mathematical ability 		T 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: rs11921590
rs11921590
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0596887
Disease:
mathematical ability 		T 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: rs1826347
rs1826347
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs1873625
rs1873625
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0596887
Disease:
mathematical ability 		C 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: rs369849874
rs369849874
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs56116382
rs56116382
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs56116382
rs56116382
Entrez Id: 8927
Gene Symbol: BSN
BSN
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: rs6770670
rs6770670
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs2172252
rs2172252
Entrez Id: 8927
Gene Symbol: BSN
BSN
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: rs116046827
rs116046827
Entrez Id: 8927
Gene Symbol: BSN
BSN
CUI: C0033860
Disease:
Psoriasis 		0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016