rs6017452
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 0 | common in complete genomics |
| Make rs6017452(C;C) |
| Make rs6017452(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 44975362 |
| Gene | STK4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6017452 |
| dbSNP (classic) | rs6017452 |
| ClinGen | rs6017452 |
| ebi | rs6017452 |
| HLI | rs6017452 |
| Exac | rs6017452 |
| Gnomad | rs6017452 |
| Varsome | rs6017452 |
| LitVar | rs6017452 |
| Map | rs6017452 |
| PheGenI | rs6017452 |
| Biobank | rs6017452 |
| 1000 genomes | rs6017452 |
| hgdp | rs6017452 |
| ensembl | rs6017452 |
| geneview | rs6017452 |
| scholar | rs6017452 |
| rs6017452 | |
| pharmgkb | rs6017452 |
| gwascentral | rs6017452 |
| openSNP | rs6017452 |
| 23andMe | rs6017452 |
| SNPshot | rs6017452 |
| SNPdbe | rs6017452 |
| MSV3d | rs6017452 |
| GWAS Ctlg | rs6017452 |
| GMAF | 0.4743 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21630024] Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
