rs477992
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs477992(A;A) |
| Make rs477992(A;G) |
| Make rs477992(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 119714953 |
| Gene | PHGDH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs477992 |
| dbSNP (classic) | rs477992 |
| ClinGen | rs477992 |
| ebi | rs477992 |
| HLI | rs477992 |
| Exac | rs477992 |
| Gnomad | rs477992 |
| Varsome | rs477992 |
| LitVar | rs477992 |
| Map | rs477992 |
| PheGenI | rs477992 |
| Biobank | rs477992 |
| 1000 genomes | rs477992 |
| hgdp | rs477992 |
| ensembl | rs477992 |
| geneview | rs477992 |
| scholar | rs477992 |
| rs477992 | |
| pharmgkb | rs477992 |
| gwascentral | rs477992 |
| openSNP | rs477992 |
| 23andMe | rs477992 |
| SNPshot | rs477992 |
| SNPdbe | rs477992 |
| MSV3d | rs477992 |
| GWAS Ctlg | rs477992 |
| GMAF | 0.2534 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21886157 |
| Trait | |
| Title | Human metabolic individuality in biomedical and pharmaceutical research. |
| Risk Allele | A |
| P-val | 3E-14 |
| Odds Ratio | 0.0510 None |
