rs6088792
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6088792(C;C) |
| Make rs6088792(C;T) |
| Make rs6088792(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 35321981 |
| Gene | UQCC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6088792 |
| dbSNP (classic) | rs6088792 |
| ClinGen | rs6088792 |
| ebi | rs6088792 |
| HLI | rs6088792 |
| Exac | rs6088792 |
| Gnomad | rs6088792 |
| Varsome | rs6088792 |
| LitVar | rs6088792 |
| Map | rs6088792 |
| PheGenI | rs6088792 |
| Biobank | rs6088792 |
| 1000 genomes | rs6088792 |
| hgdp | rs6088792 |
| ensembl | rs6088792 |
| geneview | rs6088792 |
| scholar | rs6088792 |
| rs6088792 | |
| pharmgkb | rs6088792 |
| gwascentral | rs6088792 |
| openSNP | rs6088792 |
| 23andMe | rs6088792 |
| SNPshot | rs6088792 |
| SNPdbe | rs6088792 |
| MSV3d | rs6088792 |
| GWAS Ctlg | rs6088792 |
| GMAF | 0.1938 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | T |
| P-val | 7.9999999999999996E-7 |
| Odds Ratio | 4.70 [2.74-6.66] % SD taller |
[PMID 20017971
] Assessing the impact of global versus local ancestry in association studies.
