rs16964211
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16964211(A;A) |
| Make rs16964211(A;G) |
| Make rs16964211(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 51238298 |
| Gene | CYP19A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16964211 |
| dbSNP (classic) | rs16964211 |
| ClinGen | rs16964211 |
| ebi | rs16964211 |
| HLI | rs16964211 |
| Exac | rs16964211 |
| Gnomad | rs16964211 |
| Varsome | rs16964211 |
| LitVar | rs16964211 |
| Map | rs16964211 |
| PheGenI | rs16964211 |
| Biobank | rs16964211 |
| 1000 genomes | rs16964211 |
| hgdp | rs16964211 |
| ensembl | rs16964211 |
| geneview | rs16964211 |
| scholar | rs16964211 |
| rs16964211 | |
| pharmgkb | rs16964211 |
| gwascentral | rs16964211 |
| openSNP | rs16964211 |
| 23andMe | rs16964211 |
| SNPshot | rs16964211 |
| SNPdbe | rs16964211 |
| MSV3d | rs16964211 |
| GWAS Ctlg | rs16964211 |
| GMAF | 0.1869 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20881960 ]
|
| Trait | Height |
| Title | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Risk Allele | A |
| P-val | 2E-9 |
| Odds Ratio | .05 [NR] unit decrease |
