rs4759042
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4759042(C;C) |
| Make rs4759042(C;T) |
| Make rs4759042(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 56983563 |
| Gene | UGT2B24P |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4759042 |
| dbSNP (classic) | rs4759042 |
| ClinGen | rs4759042 |
| ebi | rs4759042 |
| HLI | rs4759042 |
| Exac | rs4759042 |
| Gnomad | rs4759042 |
| Varsome | rs4759042 |
| LitVar | rs4759042 |
| Map | rs4759042 |
| PheGenI | rs4759042 |
| Biobank | rs4759042 |
| 1000 genomes | rs4759042 |
| hgdp | rs4759042 |
| ensembl | rs4759042 |
| geneview | rs4759042 |
| scholar | rs4759042 |
| rs4759042 | |
| pharmgkb | rs4759042 |
| gwascentral | rs4759042 |
| openSNP | rs4759042 |
| 23andMe | rs4759042 |
| SNPshot | rs4759042 |
| SNPdbe | rs4759042 |
| MSV3d | rs4759042 |
| GWAS Ctlg | rs4759042 |
| GMAF | 0.2328 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23793025 ]
|
| Trait | Migraine |
| Title | Genome-wide meta-analysis identifies new susceptibility loci for migraine. |
| Risk Allele | |
| P-val | 3E-6 |
| Odds Ratio | 1.05 [1.03-1.09] |
