Rs966423
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs966423 |
| PheGenI | rs966423 |
| nextbio | rs966423 |
| hapmap | rs966423 |
| 1000 genomes | rs966423 |
| hgdp | rs966423 |
| ensembl | rs966423 |
| gopubmed | rs966423 |
| geneview | rs966423 |
| scholar | rs966423 |
| rs966423 | |
| pharmgkb | rs966423 |
| gwascentral | rs966423 |
| openSNP | rs966423 |
| 23andMe | rs966423 |
| 23andMe all | rs966423 |
| SNP Nexus | |
| SNPshot | rs966423 |
| SNPdbe | rs966423 |
| MSV3d | rs966423 |
| Gene | DIRC3 |
| Chromosome | 2 |
| Orientation | plus |
| GMAF | 0.3695 |
| Position | 218310340 |
| Reference | GRCh37.p5 37.3/135 |
| Max Magnitude |
| Make rs966423(C;C) |
| Make rs966423(C;T) |
| Make rs966423(T;T) |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 22267200] |
| Trait | |
| Title | Discovery of common variants associated with low TSH levels and thyroid cancer risk. |
| Risk Allele | C |
| P-val | 1E-9 |
| Odds Ratio | 1.3400 None |
[PMID 19481195] The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.
[PMID 23659773] Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma
