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rs6131

From SNPedia

Orientationminus
Stabilizedminus
Make rs6131(A;A)
Make rs6131(A;G)
Make rs6131(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position169611647
GeneSELP
is asnp
is mentioned by
dbSNPrs6131
ebirs6131
HLIrs6131
Exacrs6131
Varsomers6131
Maprs6131
PheGenIrs6131
hapmaprs6131
1000 genomesrs6131
hgdprs6131
ensemblrs6131
gopubmedrs6131
geneviewrs6131
scholarrs6131
googlers6131
pharmgkbrs6131
gwascentralrs6131
openSNPrs6131
23andMers6131
23andMe allrs6131
SNP Nexus

SNPshotrs6131
SNPdbers6131
MSV3drs6131
GWAS Ctlgrs6131
GMAF0.214
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis


[PMID 15726497OA-icon.png] Gene-environment interaction effects on the development of immune responses in the 1st year of life.


[PMID 16820586OA-icon.png] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.


[PMID 18187665OA-icon.png] Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.


[PMID 19131662OA-icon.png] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.


[PMID 19263529OA-icon.png] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.


[PMID 19330901OA-icon.png] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.


[PMID 19404301OA-icon.png] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.


[PMID 19559392OA-icon.png] A candidate gene association study of 77 polymorphisms in migraine.


[PMID 20401335OA-icon.png] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.


[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.