{{Rsnum
|rsid=104895094
|Gene=MEFV
|Chromosome=16
|position=3243403
|Orientation=plus
|GMAF=0.003214
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MEFV
}}{{omim
|id=608107
|rsnum=104895094
|variant=0010
}}{{ClinVar
|rsid=104895094
|Reversed=1
|FwdREF=A
|FwdALT=G,T
|REF=T
|ALT=A,C
|RSPOS=3293403
|CHROM=16
|GMAF=0.0032
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000040416110100
|GENEINFO=MEFV:4210
|GENE_NAME=MEFV
|GENE_ID=4210
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.3293403T>A; NC_000016.9:g.3293403T>C
|CLNSRC=UnitÃ© mÃ©dicale des maladies autoinflammatoires; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=392; 608107.0010; 39
|CLNSIG=5
|CLNCUI=C0031069
|CLNDBN=Familial Mediterranean fever; Familial mediterranean fever, autosomal dominant
|Disease=Familial Mediterranean fever; Familial mediterranean fever
|CLNACC=RCV000083741.1; RCV000002656.1; RCV000030180.1
|Tags=RV;PM;PMC;S3D;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9968; 0.003214
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1227:C0031069:249100:342:12579009; C1851347:134610:342
|COMMON=1
}}{{PMID|9668175}} Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF).