rs28940580, MEFV

N. diseases: 17
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nephrotic Syndrome
CUI: C0027726
Disease: Nephrotic Syndrome
0.010 GeneticVariation BEFREE To our knowledge, this is the first association between FMF and the M680I mutation later complicated by nephrotic syndrome and fibrillary glomerulonephritis. 12908875 2003