rs67863238
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs67863238(C;C) |
| Make rs67863238(C;G) |
| Make rs67863238(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 48246304 |
| Gene | OR4X2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs67863238 |
| dbSNP (classic) | rs67863238 |
| ClinGen | rs67863238 |
| ebi | rs67863238 |
| HLI | rs67863238 |
| Exac | rs67863238 |
| Gnomad | rs67863238 |
| Varsome | rs67863238 |
| LitVar | rs67863238 |
| Map | rs67863238 |
| PheGenI | rs67863238 |
| Biobank | rs67863238 |
| 1000 genomes | rs67863238 |
| hgdp | rs67863238 |
| ensembl | rs67863238 |
| geneview | rs67863238 |
| scholar | rs67863238 |
| rs67863238 | |
| pharmgkb | rs67863238 |
| gwascentral | rs67863238 |
| openSNP | rs67863238 |
| 23andMe | rs67863238 |
| SNPshot | rs67863238 |
| SNPdbe | rs67863238 |
| MSV3d | rs67863238 |
| GWAS Ctlg | rs67863238 |
| Max Magnitude | 0 |
[PMID 25256078] Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study
