rs909116
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs909116(C;C) |
| Make rs909116(C;T) |
| Make rs909116(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 1920716 |
| Gene | TNNT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs909116 |
| dbSNP (classic) | rs909116 |
| ClinGen | rs909116 |
| ebi | rs909116 |
| HLI | rs909116 |
| Exac | rs909116 |
| Gnomad | rs909116 |
| Varsome | rs909116 |
| LitVar | rs909116 |
| Map | rs909116 |
| PheGenI | rs909116 |
| Biobank | rs909116 |
| 1000 genomes | rs909116 |
| hgdp | rs909116 |
| ensembl | rs909116 |
| geneview | rs909116 |
| scholar | rs909116 |
| rs909116 | |
| pharmgkb | rs909116 |
| gwascentral | rs909116 |
| openSNP | rs909116 |
| 23andMe | rs909116 |
| SNPshot | rs909116 |
| SNPdbe | rs909116 |
| MSV3d | rs909116 |
| GWAS Ctlg | rs909116 |
| GMAF | 0.4761 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20453838 ]
|
| Trait | Breast cancer |
| Title | Genome-wide association study identifies five new breast cancer susceptibility loci |
| Risk Allele | T |
| P-val | 7E-7 |
| Odds Ratio | 1.17 [1.10-1.24] |
[PMID 21445572] Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies
[PMID 32366738] Low-penetrance susceptibility variants and postmenopausal oestrogen receptor positive breast cancer.
