Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11673987
rs11673987
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.800 GeneticVariation GWASCAT High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596 2012
dbSNP: rs1858037
rs1858037
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		T 0.800 GeneticVariation GWASCAT Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs1858037
rs1858037
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		A 0.800 GeneticVariation GWASCAT Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. 30423114 2019
dbSNP: rs1876518
rs1876518
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0021053
Disease:
Immune System Diseases 		0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. 21383967 2011
dbSNP: rs1876518
rs1876518
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0004364
Disease:
Autoimmune Diseases 		0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. 21383967 2011
dbSNP: rs6546146
rs6546146
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.800 GeneticVariation GWASCAT High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596 2012
dbSNP: rs934734
rs934734
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		G 0.800 GeneticVariation GWASCAT Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans. 24782177 2014
dbSNP: rs934734
rs934734
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		G 0.800 GeneticVariation GWASCAT Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. 20453842 2010
dbSNP: rs11126034
rs11126034
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		A 0.700 GeneticVariation GWASCAT High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. 24532676 2015
dbSNP: rs140661185
rs140661185
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0002395
Disease:
Alzheimer's Disease 		A 0.700 GeneticVariation GWASCAT Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. 26830138 2016
dbSNP: rs1858036
rs1858036
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASCAT High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596 2012
dbSNP: rs2661794
rs2661794
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2661794
rs2661794
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs268134
rs268134
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
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: rs268134
rs268134
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
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: rs268134
rs268134
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966 2016
dbSNP: rs268134
rs268134
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		G 0.700 GeneticVariation GWASCAT Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. 26502338 2015
dbSNP: rs3732102
rs3732102
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
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: rs61748094
rs61748094
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62139120
rs62139120
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6731993
rs6731993
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7565437
rs7565437
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0023508
Disease:
White Blood Cell Count procedure 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7569084
rs7569084
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7569084
rs7569084
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7569084
rs7569084
Entrez Id: 200734
Gene Symbol: SPRED2
SPRED2
CUI: C0200641
Disease:
Blood basophil count (lab test) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016