rs17157903
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17157903(C;C) |
| Make rs17157903(C;T) |
| Make rs17157903(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 103987589 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17157903 |
| dbSNP (classic) | rs17157903 |
| ClinGen | rs17157903 |
| ebi | rs17157903 |
| HLI | rs17157903 |
| Exac | rs17157903 |
| Gnomad | rs17157903 |
| Varsome | rs17157903 |
| LitVar | rs17157903 |
| Map | rs17157903 |
| PheGenI | rs17157903 |
| Biobank | rs17157903 |
| 1000 genomes | rs17157903 |
| hgdp | rs17157903 |
| ensembl | rs17157903 |
| geneview | rs17157903 |
| scholar | rs17157903 |
| rs17157903 | |
| pharmgkb | rs17157903 |
| gwascentral | rs17157903 |
| openSNP | rs17157903 |
| 23andMe | rs17157903 |
| SNPshot | rs17157903 |
| SNPdbe | rs17157903 |
| MSV3d | rs17157903 |
| GWAS Ctlg | rs17157903 |
| GMAF | 0.1612 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis (age of onset) |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | NR NR |
[PMID 19639606] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.
[PMID 23563089] Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women.
