rs10199521
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs10199521(A;A) |
| Make rs10199521(A;G) |
| Make rs10199521(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 2515741 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10199521 |
| dbSNP (classic) | rs10199521 |
| ClinGen | rs10199521 |
| ebi | rs10199521 |
| HLI | rs10199521 |
| Exac | rs10199521 |
| Gnomad | rs10199521 |
| Varsome | rs10199521 |
| LitVar | rs10199521 |
| Map | rs10199521 |
| PheGenI | rs10199521 |
| Biobank | rs10199521 |
| 1000 genomes | rs10199521 |
| hgdp | rs10199521 |
| ensembl | rs10199521 |
| geneview | rs10199521 |
| scholar | rs10199521 |
| rs10199521 | |
| pharmgkb | rs10199521 |
| gwascentral | rs10199521 |
| openSNP | rs10199521 |
| 23andMe | rs10199521 |
| SNPshot | rs10199521 |
| SNPdbe | rs10199521 |
| MSV3d | rs10199521 |
| GWAS Ctlg | rs10199521 |
| GMAF | 0.2516 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21441570 ]
|
| Trait | |
| Title | Genome-wide Meta-analysis for Severe Diabetic Retinopathy |
| Risk Allele | T |
| P-val | 0.000003 |
| Odds Ratio | 1.4600 [NR] |
[PMID 27768789] Impact of Genetic Loci Identified in Genome-Wide Association Studies on Diabetic Retinopathy in Chinese Patients With Type 2 Diabetes.
