Gene: MEFV ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61752717
rs61752717
MEFV
0.010 GeneticVariation BEFREE M694V was the only variant that was significantly more common in the AS group than in the combined or individual control groups (P = 0.026 for AS patients versus healthy controls, P = 0.046 for AS patients versus RA patient controls, and P = 0.008 for AS patients versus healthy and RA patient control groups). 20533539

2010
dbSNP: rs3743930
rs3743930
MEFV
0.010 GeneticVariation BEFREE MEFV, and particularly the E148Q mutation, is an independent modifier of the clinical manifestations of RA. 15958759

2005