rs1862513, RETN

N. diseases: 11
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.010 GeneticVariation BEFREE Lack of association between RETN rs1862513 polymorphism and cardiovascular disease in rheumatoid arthritis patients. 21345288 2011