rs4846922
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4846922(C;C) |
| Make rs4846922(C;T) |
| Make rs4846922(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 230171436 |
| Gene | GALNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4846922 |
| dbSNP (classic) | rs4846922 |
| ClinGen | rs4846922 |
| ebi | rs4846922 |
| HLI | rs4846922 |
| Exac | rs4846922 |
| Gnomad | rs4846922 |
| Varsome | rs4846922 |
| LitVar | rs4846922 |
| Map | rs4846922 |
| PheGenI | rs4846922 |
| Biobank | rs4846922 |
| 1000 genomes | rs4846922 |
| hgdp | rs4846922 |
| ensembl | rs4846922 |
| geneview | rs4846922 |
| scholar | rs4846922 |
| rs4846922 | |
| pharmgkb | rs4846922 |
| gwascentral | rs4846922 |
| openSNP | rs4846922 |
| 23andMe | rs4846922 |
| SNPshot | rs4846922 |
| SNPdbe | rs4846922 |
| MSV3d | rs4846922 |
| GWAS Ctlg | rs4846922 |
| GMAF | 0.3581 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22399527 ]
|
| Trait | |
| Title | Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. |
| Risk Allele | T |
| P-val | 4E-8 |
| Odds Ratio | 0.0800 None |
