rs10768122
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10768122(A;A) |
| Make rs10768122(A;G) |
| Make rs10768122(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 35259305 |
| Gene | SLC1A2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10768122 |
| dbSNP (classic) | rs10768122 |
| ClinGen | rs10768122 |
| ebi | rs10768122 |
| HLI | rs10768122 |
| Exac | rs10768122 |
| Gnomad | rs10768122 |
| Varsome | rs10768122 |
| LitVar | rs10768122 |
| Map | rs10768122 |
| PheGenI | rs10768122 |
| Biobank | rs10768122 |
| 1000 genomes | rs10768122 |
| hgdp | rs10768122 |
| ensembl | rs10768122 |
| geneview | rs10768122 |
| scholar | rs10768122 |
| rs10768122 | |
| pharmgkb | rs10768122 |
| gwascentral | rs10768122 |
| openSNP | rs10768122 |
| 23andMe | rs10768122 |
| SNPshot | rs10768122 |
| SNPdbe | rs10768122 |
| MSV3d | rs10768122 |
| GWAS Ctlg | rs10768122 |
| GMAF | 0.3439 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22561518 ]
|
| Trait | |
| Title | Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. |
| Risk Allele | G |
| P-val | 2E-9 |
| Odds Ratio | 1.2200 None |
