rs4766578
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4766578(A;A) |
| Make rs4766578(A;T) |
| Make rs4766578(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 111466567 |
| Gene | ATXN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4766578 |
| dbSNP (classic) | rs4766578 |
| ClinGen | rs4766578 |
| ebi | rs4766578 |
| HLI | rs4766578 |
| Exac | rs4766578 |
| Gnomad | rs4766578 |
| Varsome | rs4766578 |
| LitVar | rs4766578 |
| Map | rs4766578 |
| PheGenI | rs4766578 |
| Biobank | rs4766578 |
| 1000 genomes | rs4766578 |
| hgdp | rs4766578 |
| ensembl | rs4766578 |
| geneview | rs4766578 |
| scholar | rs4766578 |
| rs4766578 | |
| pharmgkb | rs4766578 |
| gwascentral | rs4766578 |
| openSNP | rs4766578 |
| 23andMe | rs4766578 |
| SNPshot | rs4766578 |
| SNPdbe | rs4766578 |
| MSV3d | rs4766578 |
| GWAS Ctlg | rs4766578 |
| GMAF | 0.2259 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22561518 ]
|
| Trait | |
| Title | Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. |
| Risk Allele | T |
| P-val | 4E-18 |
| Odds Ratio | 1.3200 None |
