Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28940580
rs28940580
Entrez Id: 4210
Gene Symbol: MEFV
MEFV
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