rs10889569
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10889569(A;A) |
| Make rs10889569(A;T) |
| Make rs10889569(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 65620511 |
| Gene | LEPR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10889569 |
| dbSNP (classic) | rs10889569 |
| ClinGen | rs10889569 |
| ebi | rs10889569 |
| HLI | rs10889569 |
| Exac | rs10889569 |
| Gnomad | rs10889569 |
| Varsome | rs10889569 |
| LitVar | rs10889569 |
| Map | rs10889569 |
| PheGenI | rs10889569 |
| Biobank | rs10889569 |
| 1000 genomes | rs10889569 |
| hgdp | rs10889569 |
| ensembl | rs10889569 |
| geneview | rs10889569 |
| scholar | rs10889569 |
| rs10889569 | |
| pharmgkb | rs10889569 |
| gwascentral | rs10889569 |
| openSNP | rs10889569 |
| 23andMe | rs10889569 |
| SNPshot | rs10889569 |
| SNPdbe | rs10889569 |
| MSV3d | rs10889569 |
| GWAS Ctlg | rs10889569 |
| GMAF | 0.4366 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23844046 ]
|
| Trait | C-reactive protein |
| Title | Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? |
| Risk Allele | T |
| P-val | 9E-9 |
| Odds Ratio | .05 [NR] unit increase |
