{{Rsnum
|rsid=104895221
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNFRSF1A
|position=6333490
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNFRSF1A
}}{{omim
|id=191190
|rsnum=104895221
|variant=0005
}}
{{omim
|id=142680
|rsnum=104895221
}}{{ClinVar
|rsid=104895221
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=6442656
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TNFRSF1A:7132
|GENE_NAME=TNFRSF1A
|GENE_ID=7132
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.6442656A>G
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=191190.0005; 55
|CLNSIG=5
|CLNCUI=C1275126
|CLNDBN=TNF receptor-associated periodic fever syndrome (TRAPS)
|Disease=TNF receptor-associated periodic fever syndrome (TRAPS)
|CLNACC=RCV000013132.15
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1275126:142680:32960:403833009
}}{{PMID Auto
|PMID=10199409
|Title=Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes.
}}