{{Rsnum
|rsid=104895219
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNFRSF1A
|position=6333823
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNFRSF1A
}}{{omim
|id=191190
|rsnum=104895219
|variant=0002
}}
{{omim
|id=142680
|rsnum=104895219
}}{{ClinVar
|rsid=104895219
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=6442989
|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; 2
|CLNHGVS=NC_000012.11:g.6442989G>A; NC_000012.11:g.6442989G>T
|CLNSRC=OMIM Allelic Variant; UnitÃ© mÃ©dicale des maladies autoinflammatoires
|CLNORIGIN=1
|CLNSRCID=191190.0002; 53; 294
|CLNSIG=5
|CLNCUI=C1275126
|CLNDBN=TNF receptor-associated periodic fever syndrome (TRAPS)
|Disease=TNF receptor-associated periodic fever syndrome (TRAPS)
|CLNACC=RCV000013129.23; RCV000083920.1
|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.
}}

{{PMID Auto
|PMID=13130484
|Title=Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes.
}}