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rs104895245

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104895245(C;C)
Make rs104895245(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position6333794
GeneTNFRSF1A
is asnp
is mentioned by
dbSNPrs104895245
ebirs104895245
HLIrs104895245
Exacrs104895245
Varsomers104895245
Maprs104895245
PheGenIrs104895245
hapmaprs104895245
1000 genomesrs104895245
hgdprs104895245
ensemblrs104895245
gopubmedrs104895245
geneviewrs104895245
scholarrs104895245
googlers104895245
pharmgkbrs104895245
gwascentralrs104895245
openSNPrs104895245
23andMers104895245
23andMe allrs104895245
SNP Nexus

SNPshotrs104895245
SNPdbers104895245
MSV3drs104895245
GWAS Ctlgrs104895245
Max Magnitude0
ClinVar
Risk rs104895245(C;C) rs104895245(G;G)
Alt rs104895245(C;C) rs104895245(G;G)
Reference Rs104895245(T;T)
Significance Probable-Pathogenic
Disease TNF receptor-associated periodic fever syndrome (TRAPS) not provided
Variation info
Gene TNFRSF1A
CLNDBN TNF receptor-associated periodic fever syndrome (TRAPS) not provided
Reversed 1
HGVS NC_000012.11:g.6442960A>C; NC_000012.11:g.6442960A>G
CLNSRC
CLNACC RCV000083930.1, RCV000083929.1, RCV000254771.1,