{{Rsnum
|rsid=104895304
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=MVK
|position=109591275
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MVK
}}{{omim
|id=251170
|rsnum=104895304
|variant=0004
}}
{{omim
|id=260920
|rsnum=104895304
}}{{ClinVar
|rsid=104895304
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=110029080
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MVK:4598
|GENE_NAME=MVK
|GENE_ID=4598
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.110029080T>C
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=251170.0004; 83
|CLNSIG=5
|CLNCUI=C0398691; C1959626
|CLNDBN=Hyperimmunoglobulin D with periodic fever; Mevalonic aciduria
|Disease=Hyperimmunoglobulin D with periodic fever; Mevalonic aciduria
|CLNACC=RCV000012709.14; RCV000012710.14
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=C0398691:260920:343:234538002; C1959626:610377:29
}}{{PMID Auto
|PMID=10369261
|Title=Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome.
}}

{{PMID Auto
|PMID=10369262
|Title=Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.
}}

{{PMID Auto
|PMID=10417275
|Title=Identification of a mutation cluster in mevalonate kinase deficiency, including a new mutation in a patient of Mennonite ancestry.
|OA=1
}}