{{Rsnum
|rsid=121908149
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NLRP3
|position=247424504
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NLRP3
}}{{omim
|id=606416
|rsnum=121908149
|variant=0004
}}
{{omim
|id=120100
|rsnum=121908149
}}{{ClinVar
|rsid=121908149
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=247587806
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=NLRP3:114548
|GENE_NAME=NLRP3
|GENE_ID=114548
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.10:g.247587806C>T
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=606416.0004; 102
|CLNSIG=5
|CLNCUI=C0268390
|CLNDBN=Familial amyloid nephropathy with urticaria AND deafness; Familial cold urticaria
|Disease=Familial amyloid nephropathy with urticaria AND deafness; Familial cold urticaria
|CLNACC=RCV000004621.1; RCV000084171.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0268390:191900:575:15123008; C0343068:120100:47045:238687000
}}{{PMID Auto
|PMID=11687797
|Title=Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.
}}