rs961764
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs961764(C;C) |
| Make rs961764(C;G) |
| Make rs961764(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 117200993 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs961764 |
| dbSNP (classic) | rs961764 |
| ClinGen | rs961764 |
| ebi | rs961764 |
| HLI | rs961764 |
| Exac | rs961764 |
| Gnomad | rs961764 |
| Varsome | rs961764 |
| LitVar | rs961764 |
| Map | rs961764 |
| PheGenI | rs961764 |
| Biobank | rs961764 |
| 1000 genomes | rs961764 |
| hgdp | rs961764 |
| ensembl | rs961764 |
| geneview | rs961764 |
| scholar | rs961764 |
| rs961764 | |
| pharmgkb | rs961764 |
| gwascentral | rs961764 |
| openSNP | rs961764 |
| 23andMe | rs961764 |
| SNPshot | rs961764 |
| SNPdbe | rs961764 |
| MSV3d | rs961764 |
| GWAS Ctlg | rs961764 |
| GMAF | 0.3792 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | C |
| P-val | 1E-11 |
| Odds Ratio | .02 [NR] unit decrease |
