Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61752717
rs61752717
MEFV
0.100 GeneticVariation BEFREE In both cases, S1791 was in compound heterozygosity with MEFV mutation M694V, and the characteristic clinical syndrome of FMF including amyloidosis was found. 14636645

2004
dbSNP: rs61752717
rs61752717
MEFV
0.100 GeneticVariation BEFREE Amyloidosis was confirmed by renal biopsy in only two of these cases who were homozygous for M694V and compound heterozygous for M694V/M680I. 28828621

2018
dbSNP: rs61752717
rs61752717
MEFV
0.100 GeneticVariation BEFREE In conclusion, we found a higher disease severity score and higher prevalence of amyloidosis in FMF patients who were M694V mutation carriers. 18266121

2008
dbSNP: rs61752717
rs61752717
MEFV
0.100 GeneticVariation BEFREE The M694V and V726A allelic frequencies were, respectively, significantly higher and lower in the group with amyloidosis, compared to the control FMF group. 15018633

2004