Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104895091
rs104895091
T 0.700 CausalMutation CLINVAR Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). 9668175

1998

dbSNP: rs104895093
rs104895093
C 0.700 GeneticVariation CLINVAR Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). 9668175

1998

dbSNP: rs1355225244
rs1355225244
C 0.700 GeneticVariation CLINVAR Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). 9668175

1998

dbSNP: rs1355225244
rs1355225244
C 0.700 GeneticVariation CLINVAR Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF). 9781020

1998

dbSNP: rs780770024
rs780770024
A 0.700 GeneticVariation CLINVAR Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF). 9781020

1998

dbSNP: rs876660997
rs876660997
CA 0.700 GeneticVariation CLINVAR Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF). 9781020

1998

dbSNP: rs876660997
rs876660997
CA 0.700 GeneticVariation CLINVAR Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). 9668175

1998

dbSNP: rs28940578
rs28940578
T 0.900 CausalMutation CLINVAR Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. 10234504

1999

dbSNP: rs28940578
rs28940578
T 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
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
G 0.900 CausalMutation CLINVAR Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. 10234504

1999

dbSNP: rs61752717
rs61752717
C 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: rs28940580
rs28940580
T 0.890 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: rs28940580
rs28940580
G 0.890 CausalMutation CLINVAR Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. 10090880

1999

dbSNP: rs28940580
rs28940580
T 0.890 CausalMutation CLINVAR Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis. 10234504

1999

dbSNP: rs28940580
rs28940580
T 0.890 CausalMutation CLINVAR Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. 10090880

1999

dbSNP: rs104895097
rs104895097
T 0.850 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: rs104895097
rs104895097
T 0.850 CausalMutation CLINVAR Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. 10090880

1999

dbSNP: rs61732874
rs61732874
A 0.820 CausalMutation CLINVAR Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. 10090880

1999

dbSNP: rs104895091
rs104895091
T 0.700 CausalMutation CLINVAR Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. 10090880

1999

dbSNP: rs780770024
rs780770024
A 0.700 GeneticVariation 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: rs28940578
rs28940578
T 0.900 CausalMutation CLINVAR The genetic basis of autosomal dominant familial Mediterranean fever. 10787449

2000

dbSNP: rs28940578
rs28940578
T 0.900 CausalMutation CLINVAR MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever. 10612841

2000

dbSNP: rs28940579
rs28940579
G 0.900 CausalMutation CLINVAR MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever. 10612841

2000

dbSNP: rs28940579
rs28940579
G 0.900 CausalMutation CLINVAR Familial Mediterranean fever diagnosed by PCR. 10879615

2000