rs1046896
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1046896(C;C) |
| Make rs1046896(C;T) |
| Make rs1046896(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 82727657 |
| Gene | FN3KRP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1046896 |
| dbSNP (classic) | rs1046896 |
| ClinGen | rs1046896 |
| ebi | rs1046896 |
| HLI | rs1046896 |
| Exac | rs1046896 |
| Gnomad | rs1046896 |
| Varsome | rs1046896 |
| LitVar | rs1046896 |
| Map | rs1046896 |
| PheGenI | rs1046896 |
| Biobank | rs1046896 |
| 1000 genomes | rs1046896 |
| hgdp | rs1046896 |
| ensembl | rs1046896 |
| geneview | rs1046896 |
| scholar | rs1046896 |
| rs1046896 | |
| pharmgkb | rs1046896 |
| gwascentral | rs1046896 |
| openSNP | rs1046896 |
| 23andMe | rs1046896 |
| SNPshot | rs1046896 |
| SNPdbe | rs1046896 |
| MSV3d | rs1046896 |
| GWAS Ctlg | rs1046896 |
| GMAF | 0.3861 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20858683
] Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
| GWAS snp | |
|---|---|
| PMID | [PMID 24244560]
|
| Trait | Glycated hemoglobin levels |
| Title | A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry. |
| Risk Allele | T |
| P-val | 2E-7 |
| Odds Ratio | .03 [0.019-0.043] unit increase |
