rs3917657
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3917657(C;C) |
| Make rs3917657(C;T) |
| Make rs3917657(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169629504 |
| Gene | SELP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3917657 |
| dbSNP (classic) | rs3917657 |
| ClinGen | rs3917657 |
| ebi | rs3917657 |
| HLI | rs3917657 |
| Exac | rs3917657 |
| Gnomad | rs3917657 |
| Varsome | rs3917657 |
| LitVar | rs3917657 |
| Map | rs3917657 |
| PheGenI | rs3917657 |
| Biobank | rs3917657 |
| 1000 genomes | rs3917657 |
| hgdp | rs3917657 |
| ensembl | rs3917657 |
| geneview | rs3917657 |
| scholar | rs3917657 |
| rs3917657 | |
| pharmgkb | rs3917657 |
| gwascentral | rs3917657 |
| openSNP | rs3917657 |
| 23andMe | rs3917657 |
| SNPshot | rs3917657 |
| SNPdbe | rs3917657 |
| MSV3d | rs3917657 |
| GWAS Ctlg | rs3917657 |
| GMAF | 0.1125 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19404301
] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE
[PMID 32429899] Putative functional non-coding polymorphisms in SELP significantly modulate sP-selectin levels, arterial stiffness and type 2 diabetes mellitus susceptibility.
