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rs1224141

From SNPedia

Orientationplus
Stabilizedplus
Make rs1224141(G;G)
Make rs1224141(G;T)
Make rs1224141(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108283375
GeneTNFSF13B
is asnp
is mentioned by
dbSNPrs1224141
ebirs1224141
HLIrs1224141
Exacrs1224141
Varsomers1224141
Maprs1224141
PheGenIrs1224141
hapmaprs1224141
1000 genomesrs1224141
hgdprs1224141
ensemblrs1224141
gopubmedrs1224141
geneviewrs1224141
scholarrs1224141
googlers1224141
pharmgkbrs1224141
gwascentralrs1224141
openSNPrs1224141
23andMers1224141
23andMe allrs1224141
SNP Nexus

SNPshotrs1224141
SNPdbers1224141
MSV3drs1224141
GWAS Ctlgrs1224141
GMAF0.1511
Max Magnitude
? (G;G) (G;T) (T;T) 28

[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.