rs6133
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs6133(G;T) |
| Make rs6133(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169596108 |
| Gene | SELP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6133 |
| dbSNP (classic) | rs6133 |
| ClinGen | rs6133 |
| ebi | rs6133 |
| HLI | rs6133 |
| Exac | rs6133 |
| Gnomad | rs6133 |
| Varsome | rs6133 |
| LitVar | rs6133 |
| Map | rs6133 |
| PheGenI | rs6133 |
| Biobank | rs6133 |
| 1000 genomes | rs6133 |
| hgdp | rs6133 |
| ensembl | rs6133 |
| geneview | rs6133 |
| scholar | rs6133 |
| rs6133 | |
| pharmgkb | rs6133 |
| gwascentral | rs6133 |
| openSNP | rs6133 |
| 23andMe | rs6133 |
| SNPshot | rs6133 |
| SNPdbe | rs6133 |
| MSV3d | rs6133 |
| GWAS Ctlg | rs6133 |
| GMAF | 0.1993 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19404301
] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE
[PMID 19240957] Candidate gene analysis of selectin cluster in patients with multiple sclerosis
| ClinVar | |
|---|---|
| Risk | rs6133(C;C) rs6133(T;T) |
| Alt | rs6133(C;C) rs6133(T;T) |
| Reference | Rs6133(G;G) |
| Significance | Other |
| Disease | Atopy |
| Variation | info |
| Gene | SELP |
| CLNDBN | Atopy, susceptibility to |
| Reversed | 1 |
| HGVS | NC_000001.10:g.169565346C>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000014483.2, |
[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 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 19559392] A candidate gene association study of 77 polymorphisms in migraine.
[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis
