rs2749097
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2749097(C;C) |
| Make rs2749097(C;G) |
| Make rs2749097(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 63661797 |
| Gene | PGM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2749097 |
| dbSNP (classic) | rs2749097 |
| ClinGen | rs2749097 |
| ebi | rs2749097 |
| HLI | rs2749097 |
| Exac | rs2749097 |
| Gnomad | rs2749097 |
| Varsome | rs2749097 |
| LitVar | rs2749097 |
| Map | rs2749097 |
| PheGenI | rs2749097 |
| Biobank | rs2749097 |
| 1000 genomes | rs2749097 |
| hgdp | rs2749097 |
| ensembl | rs2749097 |
| geneview | rs2749097 |
| scholar | rs2749097 |
| rs2749097 | |
| pharmgkb | rs2749097 |
| gwascentral | rs2749097 |
| openSNP | rs2749097 |
| 23andMe | rs2749097 |
| SNPshot | rs2749097 |
| SNPdbe | rs2749097 |
| MSV3d | rs2749097 |
| GWAS Ctlg | rs2749097 |
| GMAF | 0.2176 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21665994 ]
|
| Trait | |
| Title | Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. |
| Risk Allele | G |
| P-val | 2E-9 |
| Odds Ratio | 0.1200 [0.08-0.16] unit decrease |
