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rs4965814

From SNPedia

Orientationplus
Stabilizedplus
Make rs4965814(C;C)
Make rs4965814(C;T)
Make rs4965814(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position101273712
GeneSELS
is asnp
is mentioned by
dbSNPrs4965814
ebirs4965814
HLIrs4965814
Exacrs4965814
Varsomers4965814
Maprs4965814
PheGenIrs4965814
hapmaprs4965814
1000 genomesrs4965814
hgdprs4965814
ensemblrs4965814
gopubmedrs4965814
geneviewrs4965814
scholarrs4965814
googlers4965814
pharmgkbrs4965814
gwascentralrs4965814
openSNPrs4965814
23andMers4965814
23andMe allrs4965814
SNP Nexus

SNPshotrs4965814
SNPdbers4965814
MSV3drs4965814
GWAS Ctlgrs4965814
GMAF0.4385
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23829426OA-icon.png] Genetic variation in Tanis was associated with elevating plasma triglyceride level in Chinese nondiabetic subjects


[PMID 23161441OA-icon.png] Polymorphisms in the Selenoprotein S gene and subclinical cardiovascular disease in the Diabetes Heart Study


[PMID 17665434OA-icon.png] Association of interleukin-6 and interleukin-10 genotypes with radiographic damage in rheumatoid arthritis is dependent on autoantibody status.


[PMID 18625033OA-icon.png] Polymorphisms in the selenoprotein S gene: lack of association with autoimmune inflammatory diseases.


[PMID 18974842OA-icon.png] Gender differences in genetic risk profiles for cardiovascular disease.


[PMID 20619427OA-icon.png] Expression of the selenoprotein S (SELS) gene in subcutaneous adipose tissue and SELS genotype are associated with metabolic risk factors.