rs2779116
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2779116(A;A) |
| Make rs2779116(A;G) |
| Make rs2779116(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 158615625 |
| Gene | SPTA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2779116 |
| dbSNP (classic) | rs2779116 |
| ClinGen | rs2779116 |
| ebi | rs2779116 |
| HLI | rs2779116 |
| Exac | rs2779116 |
| Gnomad | rs2779116 |
| Varsome | rs2779116 |
| LitVar | rs2779116 |
| Map | rs2779116 |
| PheGenI | rs2779116 |
| Biobank | rs2779116 |
| 1000 genomes | rs2779116 |
| hgdp | rs2779116 |
| ensembl | rs2779116 |
| geneview | rs2779116 |
| scholar | rs2779116 |
| rs2779116 | |
| pharmgkb | rs2779116 |
| gwascentral | rs2779116 |
| openSNP | rs2779116 |
| 23andMe | rs2779116 |
| SNPshot | rs2779116 |
| SNPdbe | rs2779116 |
| MSV3d | rs2779116 |
| GWAS Ctlg | rs2779116 |
| GMAF | 0.3067 |
| Max Magnitude | 0 |
[PMID 20858683
] Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
