rs496601
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs496601(A;A) |
| Make rs496601(A;G) |
| Make rs496601(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 58863970 |
| Gene | GLYATL2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs496601 |
| dbSNP (classic) | rs496601 |
| ClinGen | rs496601 |
| ebi | rs496601 |
| HLI | rs496601 |
| Exac | rs496601 |
| Gnomad | rs496601 |
| Varsome | rs496601 |
| LitVar | rs496601 |
| Map | rs496601 |
| PheGenI | rs496601 |
| Biobank | rs496601 |
| 1000 genomes | rs496601 |
| hgdp | rs496601 |
| ensembl | rs496601 |
| geneview | rs496601 |
| scholar | rs496601 |
| rs496601 | |
| pharmgkb | rs496601 |
| gwascentral | rs496601 |
| openSNP | rs496601 |
| 23andMe | rs496601 |
| SNPshot | rs496601 |
| SNPdbe | rs496601 |
| MSV3d | rs496601 |
| GWAS Ctlg | rs496601 |
| GMAF | 0.1171 |
| Max Magnitude | 0 |
[PMID 24194259
] Racial differences in the association of insulin-like growth factor pathway and colorectal adenoma risk
