ULK4, unc-51 like kinase 4, 54986

N. diseases: 32; N. variants: 515
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052501
rs1052501
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.810 GeneticVariation BEFREE Common single-nucleotide polymorphisms (SNPs) at 2p23.3 (rs6746082), 3p22.1 (rs1052501), 3q26.2 (rs10936599), 6p21.33 (rs2285803), 7p15.3 (rs4487645), 17p11.2 (rs4273077), and 22q13.1 (rs877529) have recently been shown to influence MM risk. 24449210 2014
dbSNP: rs1052501
rs1052501
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.810 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs1052501
rs1052501
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.810 GeneticVariation GWASCAT We identified risk loci for multiple myeloma at 3p22.1 (rs1052501 in ULK4; odds ratio (OR) = 1.32; P = 7.47 × 10(-9)) and 7p15.3 (rs4487645, OR = 1.38; P = 3.33 × 10(-15)). 22120009 2011
dbSNP: rs1052501
rs1052501
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.810 GeneticVariation GWASDB We identified risk loci for multiple myeloma at 3p22.1 (rs1052501 in ULK4; odds ratio (OR) = 1.32; P = 7.47 × 10(-9)) and 7p15.3 (rs4487645, OR = 1.38; P = 3.33 × 10(-15)). 22120009 2011
dbSNP: rs6763508
rs6763508
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.800 GeneticVariation GWASCAT Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. 28112199 2017
dbSNP: rs6599192
rs6599192
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. 27363682 2016
dbSNP: rs73071352
rs73071352
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.800 GeneticVariation GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015
dbSNP: rs2272007
rs2272007
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.800 GeneticVariation GWASCAT The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs2272007
rs2272007
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs2272007
rs2272007
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		A 0.800 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs6599175
rs6599175
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.800 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
dbSNP: rs6599175
rs6599175
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		G 0.800 GeneticVariation GWASCAT The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs6599175
rs6599175
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
dbSNP: rs2272007
rs2272007
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs6599175
rs6599175
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs6599192
rs6599192
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs6763508
rs6763508
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs73071352
rs73071352
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026764
Disease:
Multiple Myeloma 		0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011
dbSNP: rs1717027
rs1717027
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0428883
Disease:
Diastolic blood pressure 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs2683696
rs2683696
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0428883
Disease:
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs60257661
rs60257661
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6768542
rs6768542
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9816029
rs9816029
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C1305855
Disease:
Body mass index 		C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs9848754
rs9848754
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0026470
Disease:
Monoclonal Gammopathy of Undetermined Significance 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma. 30737484 2019
dbSNP: rs9848754
rs9848754
Entrez Id: 54986
Gene Symbol: ULK4
ULK4
CUI: C0030489
Disease:
Paraproteinemias 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma. 30737484 2019