{{Rsnum
|rsid=104895228
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TNFRSF1A
|position=6333764
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNFRSF1A
}}{{omim
|id=191190
|rsnum=104895228
|variant=0011
}}
{{omim
|id=142680
|rsnum=104895228
}}{{ClinVar
|rsid=104895228
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=6442930
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=TNFRSF1A:7132
|GENE_NAME=TNFRSF1A
|GENE_ID=7132
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000012.11:g.6442930A>C; NC_000012.11:g.6442930A>G; NC_000012.11:g.6442930A>T
|CLNSRC=UnitÃ© mÃ©dicale des maladies autoinflammatoires; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=353; 94; 191190.0011; 149
|CLNSIG=5
|CLNCUI=C1275126
|CLNDBN=TNF receptor-associated periodic fever syndrome (TRAPS)
|Disease=TNF receptor-associated periodic fever syndrome (TRAPS)
|CLNACC=RCV000083940.1; RCV000083939.1; RCV000013138.23
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1275126:142680:32960:403833009
}}{{PMID|11817598}} An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome.

{{PMID|14610673}} Tumour necrosis factor receptor-associated periodic syndrome with a novel mutation in the TNFRSF1A gene in a Japanese family.

{{PMID|15492850}} Novel mutations in TNFRSF1A in patients with typical tumor necrosis factor receptor-associated periodic syndrome and with systemic lupus erythematosus in Japanese.