rs1250009
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1250009(C;C) |
| Make rs1250009(C;T) |
| Make rs1250009(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 79085654 |
| Gene | ZMIZ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1250009 |
| dbSNP (classic) | rs1250009 |
| ClinGen | rs1250009 |
| ebi | rs1250009 |
| HLI | rs1250009 |
| Exac | rs1250009 |
| Gnomad | rs1250009 |
| Varsome | rs1250009 |
| LitVar | rs1250009 |
| Map | rs1250009 |
| PheGenI | rs1250009 |
| Biobank | rs1250009 |
| 1000 genomes | rs1250009 |
| hgdp | rs1250009 |
| ensembl | rs1250009 |
| geneview | rs1250009 |
| scholar | rs1250009 |
| rs1250009 | |
| pharmgkb | rs1250009 |
| gwascentral | rs1250009 |
| openSNP | rs1250009 |
| 23andMe | rs1250009 |
| SNPshot | rs1250009 |
| SNPdbe | rs1250009 |
| MSV3d | rs1250009 |
| GWAS Ctlg | rs1250009 |
| GMAF | 0.2961 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[22198471?dopt=Abstract PMID 22198471] in Chinese women rs1250009 was consistently associated with risk of breast cancer with a per-allele OR of 1.13 (95% CI 1.02-1.25)
[PMID 19838307
] Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes.
