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rs12039904

From SNPedia

Orientationplus
Stabilizedplus
Make rs12039904(C;C)
Make rs12039904(C;T)
Make rs12039904(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position173243134
GeneIGHVII-15-1
is asnp
is mentioned by
dbSNPrs12039904
ebirs12039904
HLIrs12039904
Exacrs12039904
Varsomers12039904
Maprs12039904
PheGenIrs12039904
hapmaprs12039904
1000 genomesrs12039904
hgdprs12039904
ensemblrs12039904
gopubmedrs12039904
geneviewrs12039904
scholarrs12039904
googlers12039904
pharmgkbrs12039904
gwascentralrs12039904
openSNPrs12039904
23andMers12039904
23andMe allrs12039904
SNP Nexus

SNPshotrs12039904
SNPdbers12039904
MSV3drs12039904
GWAS Ctlgrs12039904
GMAF0.1933
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19092840OA-icon.png] Replication of the TNFSF4 (OX40L) promoter region association with systemic lupus erythematosus


[PMID 22422496OA-icon.png] Independent Replication and Metaanalysis of Association Studies Establish TNFSF4 as a Susceptibility Gene Preferentially Associated with the Subset of Anticentromere-positive Patients with Systemic Sclerosis

[PMID 19778912OA-icon.png] Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis.

[PMID 21187296] A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort.


[PMID 22870213OA-icon.png] Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population.