Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56219066
rs56219066
Entrez Id: 22936
Gene Symbol: ELL2
ELL2
CUI: C0026470
Disease:
Monoclonal Gammopathy of Undetermined Significance
T 0.700 GeneticVariation GWASCAT Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. 26007630 2015