rs6599175, ULK4

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
0.800 GeneticVariation GWASDB Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. 23955597 2013
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
0.800 GeneticVariation GWASCAT The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. 23502783 2013
Multiple Myeloma
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
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
0.800 GeneticVariation GWASDB Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. 22120009 2011