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rs12583006

From SNPedia

Orientationplus
Stabilizedplus
Make rs12583006(A;A)
Make rs12583006(A;T)
Make rs12583006(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108285104
GeneTNFSF13B
is asnp
is mentioned by
dbSNPrs12583006
ebirs12583006
HLIrs12583006
Exacrs12583006
Varsomers12583006
Maprs12583006
PheGenIrs12583006
hapmaprs12583006
1000 genomesrs12583006
hgdprs12583006
ensemblrs12583006
gopubmedrs12583006
geneviewrs12583006
scholarrs12583006
googlers12583006
pharmgkbrs12583006
gwascentralrs12583006
openSNPrs12583006
23andMers12583006
23andMe allrs12583006
SNP Nexus

SNPshotrs12583006
SNPdbers12583006
MSV3drs12583006
GWAS Ctlgrs12583006
GMAF0.2769
Max Magnitude
? (A;A) (A;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.