rs3917733
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3917733(A;A) |
| Make rs3917733(A;G) |
| Make rs3917733(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169611272 |
| Gene | SELP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3917733 |
| dbSNP (classic) | rs3917733 |
| ClinGen | rs3917733 |
| ebi | rs3917733 |
| HLI | rs3917733 |
| Exac | rs3917733 |
| Gnomad | rs3917733 |
| Varsome | rs3917733 |
| LitVar | rs3917733 |
| Map | rs3917733 |
| PheGenI | rs3917733 |
| Biobank | rs3917733 |
| 1000 genomes | rs3917733 |
| hgdp | rs3917733 |
| ensembl | rs3917733 |
| geneview | rs3917733 |
| scholar | rs3917733 |
| rs3917733 | |
| pharmgkb | rs3917733 |
| gwascentral | rs3917733 |
| openSNP | rs3917733 |
| 23andMe | rs3917733 |
| SNPshot | rs3917733 |
| SNPdbe | rs3917733 |
| MSV3d | rs3917733 |
| GWAS Ctlg | rs3917733 |
| GMAF | 0.1295 |
| Max Magnitude | 0 |
Part of a haplotype linked to stroke affecting perhaps 5% of sickle cell anemia patients
[PMID 20401335
] Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
