rs2716601
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2716601(C;C) |
| Make rs2716601(C;T) |
| Make rs2716601(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 74042353 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2716601 |
| dbSNP (classic) | rs2716601 |
| ClinGen | rs2716601 |
| ebi | rs2716601 |
| HLI | rs2716601 |
| Exac | rs2716601 |
| Gnomad | rs2716601 |
| Varsome | rs2716601 |
| LitVar | rs2716601 |
| Map | rs2716601 |
| PheGenI | rs2716601 |
| Biobank | rs2716601 |
| 1000 genomes | rs2716601 |
| hgdp | rs2716601 |
| ensembl | rs2716601 |
| geneview | rs2716601 |
| scholar | rs2716601 |
| rs2716601 | |
| pharmgkb | rs2716601 |
| gwascentral | rs2716601 |
| openSNP | rs2716601 |
| 23andMe | rs2716601 |
| SNPshot | rs2716601 |
| SNPdbe | rs2716601 |
| MSV3d | rs2716601 |
| GWAS Ctlg | rs2716601 |
| GMAF | 0.4348 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22310353] |
| Trait | |
| Title | Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis. |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | None None |
