{{Rsnum
|rsid=121908154
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NLRP3
|position=247424375
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NLRP3
}}{{omim
|id=606416
|rsnum=121908154
|variant=0009
}}
{{omim
|id=120100
|rsnum=121908154
}}{{ClinVar
|rsid=121908154
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=247587677
|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.247587677T>C
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=606416.0009; 128
|CLNSIG=5
|CLNCUI=C0409818
|CLNDBN=Chronic infantile neurological, cutaneous and articular syndrome; Familial cold urticaria
|Disease=Chronic infantile neurological; Familial cold urticaria
|CLNACC=RCV000004628.1; RCV000084248.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0409818:607115:1451:239826001; C0343068:120100:47045:238687000
}}{{PMID Auto
|PMID=12032915
|Title=Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes.
|OA=1
}}