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rs10508198

From SNPedia

Orientationplus
Stabilizedplus
Make rs10508198(C;C)
Make rs10508198(C;G)
Make rs10508198(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position108290440
GeneLOC102724347, TNFSF13B
is asnp
is mentioned by
dbSNPrs10508198
ebirs10508198
HLIrs10508198
Exacrs10508198
Varsomers10508198
Maprs10508198
PheGenIrs10508198
hapmaprs10508198
1000 genomesrs10508198
hgdprs10508198
ensemblrs10508198
gopubmedrs10508198
geneviewrs10508198
scholarrs10508198
googlers10508198
pharmgkbrs10508198
gwascentralrs10508198
openSNPrs10508198
23andMers10508198
23andMe allrs10508198
SNP Nexus

SNPshotrs10508198
SNPdbers10508198
MSV3drs10508198
GWAS Ctlgrs10508198
GMAF0.1979
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19604268OA-icon.png] Association between total immunoglobulin E and antibody responses to naturally acquired Ascaris lumbricoides infection and polymorphisms of immune system-related LIG4, TNFSF13B and IRS2 genes


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