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rs9514828

From SNPedia

Orientationplus
Stabilizedplus
Make rs9514828(C;C)
Make rs9514828(C;T)
Make rs9514828(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108269025
GeneTNFSF13B
is asnp
is mentioned by
dbSNPrs9514828
ebirs9514828
HLIrs9514828
Exacrs9514828
Varsomers9514828
Maprs9514828
PheGenIrs9514828
hapmaprs9514828
1000 genomesrs9514828
hgdprs9514828
ensemblrs9514828
gopubmedrs9514828
geneviewrs9514828
scholarrs9514828
googlers9514828
pharmgkbrs9514828
gwascentralrs9514828
openSNPrs9514828
23andMers9514828
23andMe allrs9514828
SNP Nexus

SNPshotrs9514828
SNPdbers9514828
MSV3drs9514828
GWAS Ctlgrs9514828
GMAF0.3531
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23251602OA-icon.png] Variation in dicer gene is associated with increased survival in T-cell lymphoma


[PMID 23845207] B-cell activating factor genetic variants in lymphomagenesis associated with primary Sjogren's syndrome


[PMID 19051265OA-icon.png] Serum BLyS levels increase after rituximab as initial therapy in patients with follicular Grade 1 non-Hodgkin lymphoma.


[PMID 19383901OA-icon.png] Genetic variation in B-cell-activating factor is associated with an increased risk of developing B-cell non-Hodgkin lymphoma.


[PMID 22338013] Cytokine BAFF gene variation is associated with survival of patients with T-cell lymphomas.


[PMID 22928528] Expression of genes involved in susceptibility to multifactorial autoimmune diseases: estimating genotype effects.