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rs3861950

From SNPedia

Orientationplus
Stabilizedplus
Make rs3861950(C;C)
Make rs3861950(C;T)
Make rs3861950(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position173187153
GeneTNFSF4
is asnp
is mentioned by
dbSNPrs3861950
ebirs3861950
HLIrs3861950
Exacrs3861950
Varsomers3861950
Maprs3861950
PheGenIrs3861950
hapmaprs3861950
1000 genomesrs3861950
hgdprs3861950
ensemblrs3861950
gopubmedrs3861950
geneviewrs3861950
scholarrs3861950
googlers3861950
pharmgkbrs3861950
gwascentralrs3861950
openSNPrs3861950
23andMers3861950
23andMe allrs3861950
SNP Nexus

SNPshotrs3861950
SNPdbers3861950
MSV3drs3861950
GWAS Ctlgrs3861950
GMAF0.3898
Max Magnitude
? (C;C) (C;T) (T;T) 28

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

[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 23184501] TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population


[PMID 26814870] [Association between tumor necrosis factor superfamily member 4 gene polymorphism and risk of asymptomatic carotid vulnerable plaque in a Chinese population].