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rs1041569

From SNPedia

Orientationplus
Stabilizedplus
Make rs1041569(A;A)
Make rs1041569(A;T)
Make rs1041569(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position108267195
is asnp
is mentioned by
dbSNPrs1041569
ebirs1041569
HLIrs1041569
Exacrs1041569
Varsomers1041569
Maprs1041569
PheGenIrs1041569
hapmaprs1041569
1000 genomesrs1041569
hgdprs1041569
ensemblrs1041569
gopubmedrs1041569
geneviewrs1041569
scholarrs1041569
googlers1041569
pharmgkbrs1041569
gwascentralrs1041569
openSNPrs1041569
23andMers1041569
23andMe allrs1041569
SNP Nexus

SNPshotrs1041569
SNPdbers1041569
MSV3drs1041569
GWAS Ctlgrs1041569
GMAF0.1556
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 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.