rs57104699, DNAH11

N. diseases: 3
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 GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015
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
Monoclonal Gammopathy of Undetermined Significance
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
0.700 GeneticVariation GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015
Paraproteinemias
CUI: C0030489
Disease: Paraproteinemias
0.700 GeneticVariation GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015