rs11169571
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11169571(C;C) |
| Make rs11169571(C;T) |
| Make rs11169571(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 50819982 |
| Gene | ATF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11169571 |
| dbSNP (classic) | rs11169571 |
| ClinGen | rs11169571 |
| ebi | rs11169571 |
| HLI | rs11169571 |
| Exac | rs11169571 |
| Gnomad | rs11169571 |
| Varsome | rs11169571 |
| LitVar | rs11169571 |
| Map | rs11169571 |
| PheGenI | rs11169571 |
| Biobank | rs11169571 |
| 1000 genomes | rs11169571 |
| hgdp | rs11169571 |
| ensembl | rs11169571 |
| geneview | rs11169571 |
| scholar | rs11169571 |
| rs11169571 | |
| pharmgkb | rs11169571 |
| gwascentral | rs11169571 |
| openSNP | rs11169571 |
| 23andMe | rs11169571 |
| SNPshot | rs11169571 |
| SNPdbe | rs11169571 |
| MSV3d | rs11169571 |
| GWAS Ctlg | rs11169571 |
| GMAF | 0.3421 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19950226] SNPs in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high risk women
[PMID 26149214] The human ATF1 rs11169571 polymorphism increases essential hypertension risk through modifying miRNA binding
