rs17261688
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17261688(A;A) |
| Make rs17261688(A;G) |
| Make rs17261688(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 160107665 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17261688 |
| dbSNP (classic) | rs17261688 |
| ClinGen | rs17261688 |
| ebi | rs17261688 |
| HLI | rs17261688 |
| Exac | rs17261688 |
| Gnomad | rs17261688 |
| Varsome | rs17261688 |
| LitVar | rs17261688 |
| Map | rs17261688 |
| PheGenI | rs17261688 |
| Biobank | rs17261688 |
| 1000 genomes | rs17261688 |
| hgdp | rs17261688 |
| ensembl | rs17261688 |
| geneview | rs17261688 |
| scholar | rs17261688 |
| rs17261688 | |
| pharmgkb | rs17261688 |
| gwascentral | rs17261688 |
| openSNP | rs17261688 |
| 23andMe | rs17261688 |
| SNPshot | rs17261688 |
| SNPdbe | rs17261688 |
| MSV3d | rs17261688 |
| GWAS Ctlg | rs17261688 |
| GMAF | 0.06336 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23725790] |
| Trait | DNA methylation (variation) |
| Title | GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. |
| Risk Allele | G |
| P-val | 3E-6 |
| Odds Ratio | NR NR |
