rs2091766
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2091766(C;C) |
| Make rs2091766(C;T) |
| Make rs2091766(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 87545188 |
| Gene | ABCB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2091766 |
| dbSNP (classic) | rs2091766 |
| ClinGen | rs2091766 |
| ebi | rs2091766 |
| HLI | rs2091766 |
| Exac | rs2091766 |
| Gnomad | rs2091766 |
| Varsome | rs2091766 |
| LitVar | rs2091766 |
| Map | rs2091766 |
| PheGenI | rs2091766 |
| Biobank | rs2091766 |
| 1000 genomes | rs2091766 |
| hgdp | rs2091766 |
| ensembl | rs2091766 |
| geneview | rs2091766 |
| scholar | rs2091766 |
| rs2091766 | |
| pharmgkb | rs2091766 |
| gwascentral | rs2091766 |
| openSNP | rs2091766 |
| 23andMe | rs2091766 |
| SNPshot | rs2091766 |
| SNPdbe | rs2091766 |
| MSV3d | rs2091766 |
| GWAS Ctlg | rs2091766 |
| GMAF | 0.3829 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19107781] Associations between ABCB1/MDR1 gene polymorphisms and Crohn's disease: a gene-wide study in a pediatric population
[PMID 15197162
] Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene.
