rs2994809
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2994809(C;C) |
| Make rs2994809(C;T) |
| Make rs2994809(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 119809354 |
| Gene | REG4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2994809 |
| dbSNP (classic) | rs2994809 |
| ClinGen | rs2994809 |
| ebi | rs2994809 |
| HLI | rs2994809 |
| Exac | rs2994809 |
| Gnomad | rs2994809 |
| Varsome | rs2994809 |
| LitVar | rs2994809 |
| Map | rs2994809 |
| PheGenI | rs2994809 |
| Biobank | rs2994809 |
| 1000 genomes | rs2994809 |
| hgdp | rs2994809 |
| ensembl | rs2994809 |
| geneview | rs2994809 |
| scholar | rs2994809 |
| rs2994809 | |
| pharmgkb | rs2994809 |
| gwascentral | rs2994809 |
| openSNP | rs2994809 |
| 23andMe | rs2994809 |
| SNPshot | rs2994809 |
| SNPdbe | rs2994809 |
| MSV3d | rs2994809 |
| GWAS Ctlg | rs2994809 |
| GMAF | 0.1777 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23650115] Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome
