rs879882
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs879882(C;C) |
| Make rs879882(C;T) |
| Make rs879882(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 31171675 |
| Gene | POU5F1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs879882 |
| dbSNP (classic) | rs879882 |
| ClinGen | rs879882 |
| ebi | rs879882 |
| HLI | rs879882 |
| Exac | rs879882 |
| Gnomad | rs879882 |
| Varsome | rs879882 |
| LitVar | rs879882 |
| Map | rs879882 |
| PheGenI | rs879882 |
| Biobank | rs879882 |
| 1000 genomes | rs879882 |
| hgdp | rs879882 |
| ensembl | rs879882 |
| geneview | rs879882 |
| scholar | rs879882 |
| rs879882 | |
| pharmgkb | rs879882 |
| gwascentral | rs879882 |
| openSNP | rs879882 |
| 23andMe | rs879882 |
| SNPshot | rs879882 |
| SNPdbe | rs879882 |
| MSV3d | rs879882 |
| GWAS Ctlg | rs879882 |
| GMAF | 0.4334 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22528324
] Genetic Variations in Stem Cell-Related Genes and Colorectal Cancer Prognosis
[PMID 18254969] Sequence variation in the human transcription factor gene POU5F1.
[PMID 19143810] Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | |
| P-val | 2E-7 |
| Odds Ratio | NR NR |
