Have questions? Visit https://www.reddit.com/r/SNPedia

rs9514827

From SNPedia

Orientationplus
Stabilizedplus
Make rs9514827(C;C)
Make rs9514827(C;T)
Make rs9514827(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108267055
is asnp
is mentioned by
dbSNPrs9514827
ebirs9514827
HLIrs9514827
Exacrs9514827
Varsomers9514827
Maprs9514827
PheGenIrs9514827
hapmaprs9514827
1000 genomesrs9514827
hgdprs9514827
ensemblrs9514827
gopubmedrs9514827
geneviewrs9514827
scholarrs9514827
googlers9514827
pharmgkbrs9514827
gwascentralrs9514827
openSNPrs9514827
23andMers9514827
23andMe allrs9514827
SNP Nexus

SNPshotrs9514827
SNPdbers9514827
MSV3drs9514827
GWAS Ctlgrs9514827
GMAF0.3021
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[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 19390683OA-icon.png] Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk.