rs4790333
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4790333(C;C) |
| Make rs4790333(C;T) |
| Make rs4790333(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 2359409 |
| Gene | SGSM2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4790333 |
| dbSNP (classic) | rs4790333 |
| ClinGen | rs4790333 |
| ebi | rs4790333 |
| HLI | rs4790333 |
| Exac | rs4790333 |
| Gnomad | rs4790333 |
| Varsome | rs4790333 |
| LitVar | rs4790333 |
| Map | rs4790333 |
| PheGenI | rs4790333 |
| Biobank | rs4790333 |
| 1000 genomes | rs4790333 |
| hgdp | rs4790333 |
| ensembl | rs4790333 |
| geneview | rs4790333 |
| scholar | rs4790333 |
| rs4790333 | |
| pharmgkb | rs4790333 |
| gwascentral | rs4790333 |
| openSNP | rs4790333 |
| 23andMe | rs4790333 |
| SNPshot | rs4790333 |
| SNPdbe | rs4790333 |
| MSV3d | rs4790333 |
| GWAS Ctlg | rs4790333 |
| GMAF | 0.4835 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21873549 ]
|
| Trait | |
| Title | Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. |
| Risk Allele | T |
| P-val | 3E-9 |
| Odds Ratio | None None |
