rs4969169
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4969169(C;C) |
| Make rs4969169(C;T) |
| Make rs4969169(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 17 |
| Position | 78357829 |
| Gene | SOCS3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4969169 |
| dbSNP (classic) | rs4969169 |
| ClinGen | rs4969169 |
| ebi | rs4969169 |
| HLI | rs4969169 |
| Exac | rs4969169 |
| Gnomad | rs4969169 |
| Varsome | rs4969169 |
| LitVar | rs4969169 |
| Map | rs4969169 |
| PheGenI | rs4969169 |
| Biobank | rs4969169 |
| 1000 genomes | rs4969169 |
| hgdp | rs4969169 |
| ensembl | rs4969169 |
| geneview | rs4969169 |
| scholar | rs4969169 |
| rs4969169 | |
| pharmgkb | rs4969169 |
| gwascentral | rs4969169 |
| openSNP | rs4969169 |
| 23andMe | rs4969169 |
| SNPshot | rs4969169 |
| SNPdbe | rs4969169 |
| MSV3d | rs4969169 |
| GWAS Ctlg | rs4969169 |
| Max Magnitude | 0 |
[PMID 25770161] Genetic variations in the SOCS3 gene in patients with Graves' ophthalmopathy
