Gene: SP140 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASCAT Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. 28112199 2017
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASCAT Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. 28165464 2017
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease BEFREE Several variants in strong linkage disequilibrium (LD) at the SP140 locus have been associated with multiple sclerosis (MS), Crohn's disease (CD) and chronic lymphocytic leukemia (CLL). 26152201 2015
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASDB A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274 2014
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASCAT Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASDB Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. 23770605 2013
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASDB Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. 22700719 2012
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASCAT Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. 22700719 2012
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease BEFREE Polymorphisms in SP140 and ACOXL were also associated with risk of CLL. 20731705 2010
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASDB We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease GWASCAT We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 GeneticVariation disease BEFREE We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008
Entrez Id: 11262
Gene Symbol: SP140
SP140 		0.430 Biomarker disease CTD_human We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)). 18758461 2008