Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Our data suggest that M694V/V726A pyrin inflammasome mutations leading to FMF disease may contribute to gender-specific differences in microbial community structure in FMF patients. 29997616

2018

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR 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: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 GeneticVariation CLINVAR Patient management and the association of less common familial Mediterranean fever symptoms with other disorders. 23907647

2014

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE In contrast, patients having E148Q or V726A mutant allele showed fewer clinical FMF symptoms. 28483595

2017

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR Patient management and the association of less common familial Mediterranean fever symptoms with other disorders. 23907647

2014

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR A rare cause of ascites: Familial Mediterranean fever. 18386244

2008

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR Gain-of-function Pyrin mutations induce NLRP3 protein-independent interleukin-1β activation and severe autoinflammation in mice. 21600797

2011

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR The V726A mutation, although identified in FMF patients with a relatively mild phenotype, has also been detected in patients with renal amyloidosis. 15745878

2005

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 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: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE Forty-two BD patients who had no symptoms and family history for FMF and 66 healthy controls were screened for common MEFV gene mutations (E148Q, M680I, M694V, and V726A). 15903027

2005

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR Familial Mediterranean fever diagnosed by PCR. 10879615

2000

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE The increased frequency of V726A gene mutation and the rarity of amyloidosis in this study suggest that Egyptian patients may have a milder form of FMF compared to other populations. 19777236

2010

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE FMF-knockin (FMF-KI) mice that express chimeric pyrin protein with FMF mutation (MefvV726A/V726A) exhibit an autoinflammatory disorder mediated by autoactivation of the pyrin inflammasome. 30457980

2019

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 GeneticVariation CLINVAR Frequency of mutations in Mediterranean fever gene, with gender and genotype-phenotype correlations in a Turkish population. 26690517

2015

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 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

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation UNIPROT Evidence-based recommendations for the practical management of Familial Mediterranean Fever. 23742958

2013

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE In this study, the frequencies of three FMF-related MEFV mutations (M694V, M680I and V726A) were investigated in FMF patients with (AA-FMF, n = 37) and without amyloidosis (non-AA-FMF, n = 35), in patients with secondary amyloidosis related to non-FMF inflammatory conditions (S-AA, n = 19) and in a non-inflammatory control group (n = 185) by molecular genetic studies using polymerase chain reaction with the ARMS (amplification refractory mutation system) method. 15122067

2004

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE A FMF-knock-in mouse strain that expresses chimeric pyrin protein with a V726A mutation (Mefv<sup>V726A/V726A</sup>) was generated to model human FMF. 27998728

2017

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype-genotype correlation. 16627024

2007

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR The B30.2 domain of pyrin, the familial Mediterranean fever protein, interacts directly with caspase-1 to modulate IL-1beta production. 16785446

2006

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 GeneticVariation CLINVAR The B30.2 domain of pyrin, the familial Mediterranean fever protein, interacts directly with caspase-1 to modulate IL-1beta production. 16785446

2006

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. 10234504

1999

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.900 GeneticVariation BEFREE The frequencies of independent alleles, with decreasing order, were E148Q (30.7 %), M694V (26.0 %), R761H (13.5 %), V726A (13.0 %), P369S (10.5 %) and M680I (6.3 %) in FMF patients. 24071932

2014

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 GeneticVariation CLINVAR Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations. 27659338

2016

dbSNP: rs28940579
rs28940579
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
G 0.900 CausalMutation CLINVAR 'Silent' carriage of two familial Mediterranean fever gene mutations in large families with only a single identified patient. 21995303

2012