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rs2076059

From SNPedia

Orientationplus
Stabilizedplus
Make rs2076059(C;C)
Make rs2076059(C;T)
Make rs2076059(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position169729780
GeneSELE
is asnp
is mentioned by
dbSNPrs2076059
ebirs2076059
HLIrs2076059
Exacrs2076059
Varsomers2076059
Maprs2076059
PheGenIrs2076059
hapmaprs2076059
1000 genomesrs2076059
hgdprs2076059
ensemblrs2076059
gopubmedrs2076059
geneviewrs2076059
scholarrs2076059
googlers2076059
pharmgkbrs2076059
gwascentralrs2076059
openSNPrs2076059
23andMers2076059
23andMe allrs2076059
SNP Nexus

SNPshotrs2076059
SNPdbers2076059
MSV3drs2076059
GWAS Ctlgrs2076059
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 25711033] [Association between inflanummatory gene polymorphisms and the risk of myocardial infarction]


[PMID 25945941] Polymorphisms of inflammatory markers and risk of essential hypertension in Tatars from Russia


[PMID 26662939] Genotype/allelic combinations as potential predictors of myocardial infarction.