rs122555372
From SNPedia
| Orientation | plus |
| Make rs122555372(A;A) |
| Make rs122555372(A;G) |
| Make rs122555372(G;G) |
| Reference | Glycine_max_v2.0 3.1/147 |
| Chromosome | 2 |
| Position | 46428517 |
| Gene | LOC100811255 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs122555372 |
| dbSNP (classic) | rs122555372 |
| ClinGen | rs122555372 |
| ebi | rs122555372 |
| HLI | rs122555372 |
| Exac | rs122555372 |
| Gnomad | rs122555372 |
| Varsome | rs122555372 |
| LitVar | rs122555372 |
| Map | rs122555372 |
| PheGenI | rs122555372 |
| Biobank | rs122555372 |
| 1000 genomes | rs122555372 |
| hgdp | rs122555372 |
| ensembl | rs122555372 |
| geneview | rs122555372 |
| scholar | rs122555372 |
| rs122555372 | |
| pharmgkb | rs122555372 |
| gwascentral | rs122555372 |
| openSNP | rs122555372 |
| 23andMe | rs122555372 |
| SNPshot | rs122555372 |
| SNPdbe | rs122555372 |
| MSV3d | rs122555372 |
| GWAS Ctlg | rs122555372 |
| Max Magnitude | 0 |
[PMID 28101933] Associations of common variants in the SLC16A11, TCF7L2, and ABCA1 genes with pediatric-onset type 2 diabetes and related glycemic traits in families: A case-control and case-parent trio study.
