rs28940579, MEFV

N. diseases: 13
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amyloid nephropathy
CUI: C0268382
Disease: Amyloid nephropathy
0.010 GeneticVariation BEFREE Homozygotes for the M694V mutation and the complex V726A-E148Q allele are the most severely affected and often endure renal amyloidosis. 11938447 2002