rs2239610
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2239610(C;C) |
| Make rs2239610(C;G) |
| Make rs2239610(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 80955913 |
| Gene | CEP128, TSHR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2239610 |
| dbSNP (classic) | rs2239610 |
| ClinGen | rs2239610 |
| ebi | rs2239610 |
| HLI | rs2239610 |
| Exac | rs2239610 |
| Gnomad | rs2239610 |
| Varsome | rs2239610 |
| LitVar | rs2239610 |
| Map | rs2239610 |
| PheGenI | rs2239610 |
| Biobank | rs2239610 |
| 1000 genomes | rs2239610 |
| hgdp | rs2239610 |
| ensembl | rs2239610 |
| geneview | rs2239610 |
| scholar | rs2239610 |
| rs2239610 | |
| pharmgkb | rs2239610 |
| gwascentral | rs2239610 |
| openSNP | rs2239610 |
| 23andMe | rs2239610 |
| SNPshot | rs2239610 |
| SNPdbe | rs2239610 |
| MSV3d | rs2239610 |
| GWAS Ctlg | rs2239610 |
| GMAF | 0.2163 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 19438904] Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease
