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rs1234314

From SNPedia

Orientationplus
Stabilizedplus
Make rs1234314(C;C)
Make rs1234314(C;G)
Make rs1234314(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position173208253
GeneTNFSF4
is asnp
is mentioned by
dbSNPrs1234314
ebirs1234314
HLIrs1234314
Exacrs1234314
Varsomers1234314
Maprs1234314
PheGenIrs1234314
hapmaprs1234314
1000 genomesrs1234314
hgdprs1234314
ensemblrs1234314
gopubmedrs1234314
geneviewrs1234314
scholarrs1234314
googlers1234314
pharmgkbrs1234314
gwascentralrs1234314
openSNPrs1234314
23andMers1234314
23andMe allrs1234314
SNP Nexus

SNPshotrs1234314
SNPdbers1234314
MSV3drs1234314
GWAS Ctlgrs1234314
GMAF0.382
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19778912OA-icon.png] Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis


[PMID 21402531] [Association study between TNFSF4 and coronary heart disease]


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


[PMID 21445270OA-icon.png] A common polymorphism in the promoter region of the TNFSF4 gene is associated with lower allele-specific expression and risk of myocardial infarction.


[PMID 23874208OA-icon.png] Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4


[PMID 24595151] Absence of association between atherosclerotic cerebral infarction and TNFSF4/TNFRSF4 single nucleotide polymorphisms rs1234313, rs1234314 and rs17568 in a Chinese population


[PMID 27088737] Genetic risk of TNFSF4 and FAM167A-BLK polymorphisms in children with asthma and allergic rhinitis in a Han Chinese population.