{{Rsnum
|rsid=104895564
|Gene=NLRP12
|Chromosome=19
|position=53810809
|Orientation=plus
|GMAF=0.005969
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NLRP12
}}{{omim
|id=609648
|rsnum=104895564
|variant=0001
}}{{ClinVar
|rsid=104895564
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=54314063
|CHROM=19
|GMAF=0.0064
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000040416110100
|GENEINFO=NLRP12:91662
|GENE_NAME=NLRP12
|GENE_ID=91662
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.54314063G>A
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=609648.0001; 723
|CLNSIG=5
|CLNCUI=C2673198
|CLNDBN=Familial cold autoinflammatory syndrome 2; not provided
|Disease=Familial cold autoinflammatory syndrome 2; not provided
|CLNACC=RCV000001663.1; RCV000084149.1
|Tags=RV;PM;PMC;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.994; 0.005969
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2673198:611762
|COMMON=1
}}{{PMID Auto
|PMID=18230725
|Title=Mutations in NALP12 cause hereditary periodic fever syndromes.
|OA=1
}}