rs2048722
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2048722(C;C) |
| Make rs2048722(C;T) |
| Make rs2048722(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 1492028 |
| Gene | TPO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2048722 |
| dbSNP (classic) | rs2048722 |
| ClinGen | rs2048722 |
| ebi | rs2048722 |
| HLI | rs2048722 |
| Exac | rs2048722 |
| Gnomad | rs2048722 |
| Varsome | rs2048722 |
| LitVar | rs2048722 |
| Map | rs2048722 |
| PheGenI | rs2048722 |
| Biobank | rs2048722 |
| 1000 genomes | rs2048722 |
| hgdp | rs2048722 |
| ensembl | rs2048722 |
| geneview | rs2048722 |
| scholar | rs2048722 |
| rs2048722 | |
| pharmgkb | rs2048722 |
| gwascentral | rs2048722 |
| openSNP | rs2048722 |
| 23andMe | rs2048722 |
| SNPshot | rs2048722 |
| SNPdbe | rs2048722 |
| MSV3d | rs2048722 |
| GWAS Ctlg | rs2048722 |
| GMAF | 0.461 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23754668] TPO genetic variants and risk of differentiated thyroid carcinoma in two European populations
