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rs17568

From SNPedia

Orientationminus
Stabilizedminus
Make rs17568(A;A)
Make rs17568(A;G)
Make rs17568(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position1212042
GeneTNFRSF4
is asnp
is mentioned by
dbSNPrs17568
ebirs17568
HLIrs17568
Exacrs17568
Varsomers17568
Maprs17568
PheGenIrs17568
hapmaprs17568
1000 genomesrs17568
hgdprs17568
ensemblrs17568
gopubmedrs17568
geneviewrs17568
scholarrs17568
googlers17568
pharmgkbrs17568
gwascentralrs17568
openSNPrs17568
23andMers17568
23andMe allrs17568
SNP Nexus

SNPshotrs17568
SNPdbers17568
MSV3drs17568
GWAS Ctlgrs17568
GMAF0.4559
Max Magnitude

[PMID 24595151] Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population [PMID 18798503] [Correlation of OX40 gene rs17568A/G polymorphism with acute coronary syndrome in Chinese Han population].


[PMID 18987746OA-icon.png] Association of interacting genes in the toll-like receptor signaling pathway and the antibody response to pertussis vaccination.


[PMID 21476935] Association of OX40 and OX40L gene polymorphisms with acute coronary syndrome in a Han Chinese population.


[PMID 23216302OA-icon.png] Genetic variation in the OX40L/OX40 system and plasma lipid and lipoprotein levels in a Chinese hypertriglyceridemic population. [PMID 26755473] Lack of Association Between rs17568 Polymorphism in OX40 Gene and Myocardial Infarction, Southern of Iran.