Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61752717
rs61752717
0.030 GeneticVariation BEFREE MEFV mutation was M694V homozygous or compound heterozygous in 52%, and simple heterozygous in 18%.Six patients had AA amyloidosis. 27838405

2017

dbSNP: rs61752717
rs61752717
0.030 GeneticVariation BEFREE The M694V homo</span>zygosity and heterozygosity were associated with increased risk of AA amyloidosis, but this association did not reach statistical significance (odds ratio 2.43; 95 % CI 0.87-6.76, and 3.33; 0.91-12.1, respectively). 25586652

2015

dbSNP: rs61752717
rs61752717
0.030 GeneticVariation BEFREE MEFV mutations are found to be increased both in FMF and non-FMF associated secondary amyloidosis in our study; however, no clear association between M694V and amyloidosis is observed, except in the non-FMF group. 15122067

2004