Rs2439302
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2439302 |
| PheGenI | rs2439302 |
| nextbio | rs2439302 |
| hapmap | rs2439302 |
| 1000 genomes | rs2439302 |
| hgdp | rs2439302 |
| ensembl | rs2439302 |
| gopubmed | rs2439302 |
| geneview | rs2439302 |
| scholar | rs2439302 |
| rs2439302 | |
| pharmgkb | rs2439302 |
| gwascentral | rs2439302 |
| openSNP | rs2439302 |
| 23andMe | rs2439302 |
| 23andMe all | rs2439302 |
| SNP Nexus | |
| SNPshot | rs2439302 |
| SNPdbe | rs2439302 |
| MSV3d | rs2439302 |
| Gene | NRG1 |
| Chromosome | 8 |
| Orientation | minus |
| GMAF | 0.4016 |
| Position | 32432369 |
| Reference | GRCh37.p5 37.3/135 |
| Max Magnitude |
| Make rs2439302(C;C) |
| Make rs2439302(C;G) |
| Make rs2439302(G;G) |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
| GWAS snp | |
|---|---|
| PMID | [PMID 22267200] |
| Trait | |
| Title | Discovery of common variants associated with low TSH levels and thyroid cancer risk. |
| Risk Allele | G |
| P-val | 2E-9 |
| Odds Ratio | 1.3600 None |
[PMID 23659773] Cumulative Risk Impact of Five Genetic Variants Associated With Papillary Thyroid Carcinoma
