rs12474201
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12474201(A;A) |
| Make rs12474201(A;G) |
| Make rs12474201(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 46694146 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12474201 |
| dbSNP (classic) | rs12474201 |
| ClinGen | rs12474201 |
| ebi | rs12474201 |
| HLI | rs12474201 |
| Exac | rs12474201 |
| Gnomad | rs12474201 |
| Varsome | rs12474201 |
| LitVar | rs12474201 |
| Map | rs12474201 |
| PheGenI | rs12474201 |
| Biobank | rs12474201 |
| 1000 genomes | rs12474201 |
| hgdp | rs12474201 |
| ensembl | rs12474201 |
| geneview | rs12474201 |
| scholar | rs12474201 |
| rs12474201 | |
| pharmgkb | rs12474201 |
| gwascentral | rs12474201 |
| openSNP | rs12474201 |
| 23andMe | rs12474201 |
| SNPshot | rs12474201 |
| SNPdbe | rs12474201 |
| MSV3d | rs12474201 |
| GWAS Ctlg | rs12474201 |
| GMAF | 0.2585 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 3E-13 |
| Odds Ratio | 0.0300 [NR] meters increase |
