rs6569479
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6569479(C;C) |
| Make rs6569479(C;T) |
| Make rs6569479(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 127285443 |
| Gene | RNF146 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6569479 |
| dbSNP (classic) | rs6569479 |
| ClinGen | rs6569479 |
| ebi | rs6569479 |
| HLI | rs6569479 |
| Exac | rs6569479 |
| Gnomad | rs6569479 |
| Varsome | rs6569479 |
| LitVar | rs6569479 |
| Map | rs6569479 |
| PheGenI | rs6569479 |
| Biobank | rs6569479 |
| 1000 genomes | rs6569479 |
| hgdp | rs6569479 |
| ensembl | rs6569479 |
| geneview | rs6569479 |
| scholar | rs6569479 |
| rs6569479 | |
| pharmgkb | rs6569479 |
| gwascentral | rs6569479 |
| openSNP | rs6569479 |
| 23andMe | rs6569479 |
| SNPshot | rs6569479 |
| SNPdbe | rs6569479 |
| MSV3d | rs6569479 |
| GWAS Ctlg | rs6569479 |
| GMAF | 0.2603 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19856316] Low risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients
[PMID 18326623
] Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.
