rs16926246
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16926246(C;C) |
| Make rs16926246(C;T) |
| Make rs16926246(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 69333636 |
| Gene | HK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16926246 |
| dbSNP (classic) | rs16926246 |
| ClinGen | rs16926246 |
| ebi | rs16926246 |
| HLI | rs16926246 |
| Exac | rs16926246 |
| Gnomad | rs16926246 |
| Varsome | rs16926246 |
| LitVar | rs16926246 |
| Map | rs16926246 |
| PheGenI | rs16926246 |
| Biobank | rs16926246 |
| 1000 genomes | rs16926246 |
| hgdp | rs16926246 |
| ensembl | rs16926246 |
| geneview | rs16926246 |
| scholar | rs16926246 |
| rs16926246 | |
| pharmgkb | rs16926246 |
| gwascentral | rs16926246 |
| openSNP | rs16926246 |
| 23andMe | rs16926246 |
| SNPshot | rs16926246 |
| SNPdbe | rs16926246 |
| MSV3d | rs16926246 |
| GWAS Ctlg | rs16926246 |
| GMAF | 0.09963 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19862010 ]
|
| Trait | Hematocrit |
| Title | Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium |
| Risk Allele | T |
| P-val | 1E-13 |
| Odds Ratio | 0.33 [0.24-0.42] % increase |
[PMID 20858683] Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
