Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Despite evidence that environmental factors (EFs) and genetic factors, including MEFV mutations (such as M694V, E148Q) and background modifier genes (MGs), affect the clinical manifestations of FMF, the relative contribution of each remains unknown. 22019429

2012

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population. 11464248

2001

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 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
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE The allele frequency of M694V among the FMF patients with radiographic sacroiliitis was significantly higher in comparison with those without sacroiliitis (OR 4.3). 23356447

2013

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE We report on a familial Mediterranean fever (FMF) patient homozygous for p.M694V in the MEFV gene who developed chronic myelomonocytic leukemia (CMML) leading to an uncontrolled and fatal inflammatory syndrome. 26076658

2015

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Pulmonary manifestations during FMF attacks are significantly more common in the Jewish population bearing the M694V mutation. 12746942

2003

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR Screening for the M694V mutation of the familial Mediterranean fever (FMF) gene in 604 French patients. 21290976

2010

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Homozygote mutation of M694V was detected in 37 (20.2%) and 4 (5.2%) patients in early onset FMF and adult onset FMF groups, respectively (p < 0.05). 19641922

2010

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Furthermore, the MEFV gene-mediated inflammatory pathway increased serum acute phase reactants, and the changes in the R202Q and M694V could play a role in inflammatory-genetic diseases, such as FMF, FMF-associated amyloidosis and chronic periodontitis. 28590056

2017

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Two hundred sixteen children who met the clinical criteria for FMF underwent molecular genetic studies to detect the 3 most common mutations in the Israeli FMF patient population (M694V, V726A, E148Q). 12508410

2003

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE The discovery of the gene responsible for FMF, Mediterranean fever gene (MEFV), and of associated mutations represents a major advance that now allows researchers to establish a strong, although nonexclusive association between one specific mutation, M694V, and the amyloid phenotype. 10647956

2000

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Both were found in compound heterozygosity with the mutation M694V in single Turkish patients with clinical syndromes characteristic for FMF. 11470495

2001

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium. 9288758

1997

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR 'Silent' carriage of two familial Mediterranean fever gene mutations in large families with only a single identified patient. 21995303

2012

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR Here, we report the different clinical courses of FMF in a family carrying the same M694V mutation. 22790142

2012

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE All 12 common mutations in the MEFV gene were analyzed and the M694V variant was found to be associated with an adverse FMF clinical outcome in the Armenian-American population, manifested by earlier onset of disease, increased severity of disease, and renal amyloidosis. 23038988

2013

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR The genetic basis of autosomal dominant familial Mediterranean fever. 10787449

2000

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications. 10364520

1999

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Study of the mutation M694V of familial Mediterranean fever in Jews. 11336402

2001

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE They also show that M694V is the most common mutation in Arab patients with FMF and seems to have an association with the development of amyloidosis and the PFMS. 15942916

2005

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Patients with FMF amyloidosis carried only M694V mutations in the FMF gene, while FMF without amyloidosis featured other mutations as well. 22675837

2012

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE The data supported the findings in literature that FMF patients with M694V homozygote and compound heterozygote for M694V gene mutations experience a more severe clinical course. 19115056

2009

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE These results indicate that the presence of homozygous M694V gene mutation seems to increase the risk for periodontitis in FMF patients. 26400644

2016

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
C 0.900 CausalMutation CLINVAR They also show that M694V is the most common mutation in Arab patients with FMF and seems to have an association with the development of amyloidosis and the PFMS. 15942916

2005

dbSNP: rs61752717
rs61752717
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Common MEFV mutation patterns were E148Q/M694I (25.0%), M694I alone (17.5%), and L110P/E148Q/M694I (17.5%), and no patient carried the M694V mutation, the most common mutation in Mediterranean patients with FMF. 19531756

2009