rs6131
| Orientation | minus |
| Stabilized | minus |
| Make rs6131(A;A) |
| Make rs6131(A;G) |
| Make rs6131(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169611647 |
| Gene | SELP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6131 |
| dbSNP (classic) | rs6131 |
| ClinGen | rs6131 |
| ebi | rs6131 |
| HLI | rs6131 |
| Exac | rs6131 |
| Gnomad | rs6131 |
| Varsome | rs6131 |
| LitVar | rs6131 |
| Map | rs6131 |
| PheGenI | rs6131 |
| Biobank | rs6131 |
| 1000 genomes | rs6131 |
| hgdp | rs6131 |
| ensembl | rs6131 |
| geneview | rs6131 |
| scholar | rs6131 |
| rs6131 | |
| pharmgkb | rs6131 |
| gwascentral | rs6131 |
| openSNP | rs6131 |
| 23andMe | rs6131 |
| SNPshot | rs6131 |
| SNPdbe | rs6131 |
| MSV3d | rs6131 |
| GWAS Ctlg | rs6131 |
| GMAF | 0.214 |
| Max Magnitude | 0 |
| ? | (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 15726497
] Gene-environment interaction effects on the development of immune responses in the 1st year of life.
[PMID 16820586] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.
[PMID 18187665] Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease.
[PMID 19131662] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
[PMID 19263529] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.
[PMID 19330901] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.
[PMID 19404301] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE.
[PMID 19559392] A candidate gene association study of 77 polymorphisms in migraine.
[PMID 20401335] 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.
