Rs116909374
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs116909374 |
| PheGenI | rs116909374 |
| nextbio | rs116909374 |
| hapmap | rs116909374 |
| 1000 genomes | rs116909374 |
| hgdp | rs116909374 |
| ensembl | rs116909374 |
| gopubmed | rs116909374 |
| geneview | rs116909374 |
| scholar | rs116909374 |
| rs116909374 | |
| pharmgkb | rs116909374 |
| gwascentral | rs116909374 |
| openSNP | rs116909374 |
| 23andMe | rs116909374 |
| 23andMe all | rs116909374 |
| SNP Nexus | |
| SNPshot | rs116909374 |
| SNPdbe | rs116909374 |
| MSV3d | rs116909374 |
| Chromosome | 14 |
| Orientation | plus |
| GMAF | 0.0192 |
| Position | 36738361 |
| Reference | GRCh37.p5 37.3/135 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs116909374(C;T) |
| Make rs116909374(T;T) |
| GWAS snp | |
|---|---|
| PMID | [PMID 22267200] |
| Trait | |
| Title | Discovery of common variants associated with low TSH levels and thyroid cancer risk. |
| Risk Allele | T |
| P-val | 5E-11 |
| Odds Ratio | 2.0900 None |
[PMID 23659773] Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma
