rs7405696
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7405696(C;C) |
| Make rs7405696(C;G) |
| Make rs7405696(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 37742044 |
| Gene | HNF1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7405696 |
| dbSNP (classic) | rs7405696 |
| ClinGen | rs7405696 |
| ebi | rs7405696 |
| HLI | rs7405696 |
| Exac | rs7405696 |
| Gnomad | rs7405696 |
| Varsome | rs7405696 |
| LitVar | rs7405696 |
| Map | rs7405696 |
| PheGenI | rs7405696 |
| Biobank | rs7405696 |
| 1000 genomes | rs7405696 |
| hgdp | rs7405696 |
| ensembl | rs7405696 |
| geneview | rs7405696 |
| scholar | rs7405696 |
| rs7405696 | |
| pharmgkb | rs7405696 |
| gwascentral | rs7405696 |
| openSNP | rs7405696 |
| 23andMe | rs7405696 |
| SNPshot | rs7405696 |
| SNPdbe | rs7405696 |
| MSV3d | rs7405696 |
| GWAS Ctlg | rs7405696 |
| GMAF | 0.4059 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21576123
] Large-scale fine mapping of the HNF1B locus and prostate cancer risk[PMID 18701471] Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.
