rs1569788
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1569788(C;C) |
| Make rs1569788(C;T) |
| Make rs1569788(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 152007481 |
| Gene | ESR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1569788 |
| dbSNP (classic) | rs1569788 |
| ClinGen | rs1569788 |
| ebi | rs1569788 |
| HLI | rs1569788 |
| Exac | rs1569788 |
| Gnomad | rs1569788 |
| Varsome | rs1569788 |
| LitVar | rs1569788 |
| Map | rs1569788 |
| PheGenI | rs1569788 |
| Biobank | rs1569788 |
| 1000 genomes | rs1569788 |
| hgdp | rs1569788 |
| ensembl | rs1569788 |
| geneview | rs1569788 |
| scholar | rs1569788 |
| rs1569788 | |
| pharmgkb | rs1569788 |
| gwascentral | rs1569788 |
| openSNP | rs1569788 |
| 23andMe | rs1569788 |
| SNPshot | rs1569788 |
| SNPdbe | rs1569788 |
| MSV3d | rs1569788 |
| GWAS Ctlg | rs1569788 |
| GMAF | 0.4132 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18305958
] 577 African American individuals with T2DM-ESRD and 596 AA controls.
- rs1569788 (nominal P = 0.000754, adjusted P = 0.0278)
[PMID 20797716] Epistasis between CYP19A1 and ESR1 polymorphisms is associated with premature ovarian failure
[PMID 18654799] Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.
