rs7644516
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7644516(A;A) |
| Make rs7644516(A;G) |
| Make rs7644516(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 25880794 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7644516 |
| dbSNP (classic) | rs7644516 |
| ClinGen | rs7644516 |
| ebi | rs7644516 |
| HLI | rs7644516 |
| Exac | rs7644516 |
| Gnomad | rs7644516 |
| Varsome | rs7644516 |
| LitVar | rs7644516 |
| Map | rs7644516 |
| PheGenI | rs7644516 |
| Biobank | rs7644516 |
| 1000 genomes | rs7644516 |
| hgdp | rs7644516 |
| ensembl | rs7644516 |
| geneview | rs7644516 |
| scholar | rs7644516 |
| rs7644516 | |
| pharmgkb | rs7644516 |
| gwascentral | rs7644516 |
| openSNP | rs7644516 |
| 23andMe | rs7644516 |
| SNPshot | rs7644516 |
| SNPdbe | rs7644516 |
| MSV3d | rs7644516 |
| GWAS Ctlg | rs7644516 |
| GMAF | 0.06841 |
| 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 | 4E-6 |
| Odds Ratio | NR NR |
[PMID 21281506
] A unified framework for multi-locus association analysis of both common and rare variants.
