rs7763064
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7763064(A;A) |
| Make rs7763064(A;G) |
| Make rs7763064(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 142476152 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7763064 |
| dbSNP (classic) | rs7763064 |
| ClinGen | rs7763064 |
| ebi | rs7763064 |
| HLI | rs7763064 |
| Exac | rs7763064 |
| Gnomad | rs7763064 |
| Varsome | rs7763064 |
| LitVar | rs7763064 |
| Map | rs7763064 |
| PheGenI | rs7763064 |
| Biobank | rs7763064 |
| 1000 genomes | rs7763064 |
| hgdp | rs7763064 |
| ensembl | rs7763064 |
| geneview | rs7763064 |
| scholar | rs7763064 |
| rs7763064 | |
| pharmgkb | rs7763064 |
| gwascentral | rs7763064 |
| openSNP | rs7763064 |
| 23andMe | rs7763064 |
| SNPshot | rs7763064 |
| SNPdbe | rs7763064 |
| MSV3d | rs7763064 |
| GWAS Ctlg | rs7763064 |
| GMAF | 0.3921 |
| 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 | 1E-33 |
| Odds Ratio | .05 [NR] unit decrease |
