rs2814944
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2814944(A;A) |
| Make rs2814944(A;G) |
| Make rs2814944(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 34585020 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2814944 |
| dbSNP (classic) | rs2814944 |
| ClinGen | rs2814944 |
| ebi | rs2814944 |
| HLI | rs2814944 |
| Exac | rs2814944 |
| Gnomad | rs2814944 |
| Varsome | rs2814944 |
| LitVar | rs2814944 |
| Map | rs2814944 |
| PheGenI | rs2814944 |
| Biobank | rs2814944 |
| 1000 genomes | rs2814944 |
| hgdp | rs2814944 |
| ensembl | rs2814944 |
| geneview | rs2814944 |
| scholar | rs2814944 |
| rs2814944 | |
| pharmgkb | rs2814944 |
| gwascentral | rs2814944 |
| openSNP | rs2814944 |
| 23andMe | rs2814944 |
| SNPshot | rs2814944 |
| SNPdbe | rs2814944 |
| MSV3d | rs2814944 |
| GWAS Ctlg | rs2814944 |
| GMAF | 0.1382 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20686565 ]
|
| Trait | |
| Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
| Risk Allele | A |
| P-val | 4E-9 |
| Odds Ratio | 0.4900 None |
[PMID 18535201] A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.
