rs6175900
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6175900(A;A) |
| Make rs6175900(A;G) |
| Make rs6175900(G;G) |
| Reference | GRCm38.p1 38.2/138 |
| Chromosome | 3 |
| Position | 101217074 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6175900 |
| dbSNP (classic) | rs6175900 |
| ClinGen | rs6175900 |
| ebi | rs6175900 |
| HLI | rs6175900 |
| Exac | rs6175900 |
| Gnomad | rs6175900 |
| Varsome | rs6175900 |
| LitVar | rs6175900 |
| Map | rs6175900 |
| PheGenI | rs6175900 |
| Biobank | rs6175900 |
| 1000 genomes | rs6175900 |
| hgdp | rs6175900 |
| ensembl | rs6175900 |
| geneview | rs6175900 |
| scholar | rs6175900 |
| rs6175900 | |
| pharmgkb | rs6175900 |
| gwascentral | rs6175900 |
| openSNP | rs6175900 |
| 23andMe | rs6175900 |
| SNPshot | rs6175900 |
| SNPdbe | rs6175900 |
| MSV3d | rs6175900 |
| GWAS Ctlg | rs6175900 |
| Max Magnitude | 0 |
[PMID 25293881
] The Contribution of Common Genetic Variation to Nicotine and Cotinine Glucuronidation in Multiple Ethnic/Racial Populations
