rs28940578, MEFV

N. diseases: 16
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Erysipelas
CUI: C0014733
Disease: Erysipelas
0.010 GeneticVariation BEFREE M694V and M694I mutations were associated with severe phenotypes, with many patients presenting with uncommon clinical manifestations such as erysipelas-like erythema or renal disturbances. 18177465 2008