rs6917747
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common on affy axiom data |
| Make rs6917747(A;A) |
| Make rs6917747(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 159981673 |
| Gene | IGF2R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6917747 |
| dbSNP (classic) | rs6917747 |
| ClinGen | rs6917747 |
| ebi | rs6917747 |
| HLI | rs6917747 |
| Exac | rs6917747 |
| Gnomad | rs6917747 |
| Varsome | rs6917747 |
| LitVar | rs6917747 |
| Map | rs6917747 |
| PheGenI | rs6917747 |
| Biobank | rs6917747 |
| 1000 genomes | rs6917747 |
| hgdp | rs6917747 |
| ensembl | rs6917747 |
| geneview | rs6917747 |
| scholar | rs6917747 |
| rs6917747 | |
| pharmgkb | rs6917747 |
| gwascentral | rs6917747 |
| openSNP | rs6917747 |
| 23andMe | rs6917747 |
| SNPshot | rs6917747 |
| SNPdbe | rs6917747 |
| MSV3d | rs6917747 |
| GWAS Ctlg | rs6917747 |
| GMAF | 0.07668 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Brain lesion load |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | NR NR |
[PMID 19307593] Signals of recent positive selection in a worldwide sample of human populations.
