rs749052
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common on affy axiom data |
| Make rs749052(A;G) |
| Make rs749052(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 231931900 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs749052 |
| dbSNP (classic) | rs749052 |
| ClinGen | rs749052 |
| ebi | rs749052 |
| HLI | rs749052 |
| Exac | rs749052 |
| Gnomad | rs749052 |
| Varsome | rs749052 |
| LitVar | rs749052 |
| Map | rs749052 |
| PheGenI | rs749052 |
| Biobank | rs749052 |
| 1000 genomes | rs749052 |
| hgdp | rs749052 |
| ensembl | rs749052 |
| geneview | rs749052 |
| scholar | rs749052 |
| rs749052 | |
| pharmgkb | rs749052 |
| gwascentral | rs749052 |
| openSNP | rs749052 |
| 23andMe | rs749052 |
| SNPshot | rs749052 |
| SNPdbe | rs749052 |
| MSV3d | rs749052 |
| GWAS Ctlg | rs749052 |
| GMAF | 0.05923 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | A |
| P-val | 9.9999999999999995E-7 |
| Odds Ratio | 8.70 [5.17-12.23] % SD taller |
[PMID 18471798
] Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.
[PMID 19570815] A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.
[PMID 20017971] Assessing the impact of global versus local ancestry in association studies.
