rs1004689
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1004689(G;G) |
| Make rs1004689(G;T) |
| Make rs1004689(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 48256185 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1004689 |
| dbSNP (classic) | rs1004689 |
| ClinGen | rs1004689 |
| ebi | rs1004689 |
| HLI | rs1004689 |
| Exac | rs1004689 |
| Gnomad | rs1004689 |
| Varsome | rs1004689 |
| LitVar | rs1004689 |
| Map | rs1004689 |
| PheGenI | rs1004689 |
| Biobank | rs1004689 |
| 1000 genomes | rs1004689 |
| hgdp | rs1004689 |
| ensembl | rs1004689 |
| geneview | rs1004689 |
| scholar | rs1004689 |
| rs1004689 | |
| pharmgkb | rs1004689 |
| gwascentral | rs1004689 |
| openSNP | rs1004689 |
| 23andMe | rs1004689 |
| SNPshot | rs1004689 |
| SNPdbe | rs1004689 |
| MSV3d | rs1004689 |
| GWAS Ctlg | rs1004689 |
| GMAF | 0.4945 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 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 | 2E-6 |
| Odds Ratio | NR NR |
