rs9596905
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9596905(A;A) |
| Make rs9596905(A;G) |
| Make rs9596905(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 54059238 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9596905 |
| dbSNP (classic) | rs9596905 |
| ClinGen | rs9596905 |
| ebi | rs9596905 |
| HLI | rs9596905 |
| Exac | rs9596905 |
| Gnomad | rs9596905 |
| Varsome | rs9596905 |
| LitVar | rs9596905 |
| Map | rs9596905 |
| PheGenI | rs9596905 |
| Biobank | rs9596905 |
| 1000 genomes | rs9596905 |
| hgdp | rs9596905 |
| ensembl | rs9596905 |
| geneview | rs9596905 |
| scholar | rs9596905 |
| rs9596905 | |
| pharmgkb | rs9596905 |
| gwascentral | rs9596905 |
| openSNP | rs9596905 |
| 23andMe | rs9596905 |
| SNPshot | rs9596905 |
| SNPdbe | rs9596905 |
| MSV3d | rs9596905 |
| GWAS Ctlg | rs9596905 |
| GMAF | 0.1286 |
| 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 | A |
| P-val | 2E-6 |
| Odds Ratio | NR NR |
