rs9395066
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9395066(A;A) |
| Make rs9395066(A;C) |
| Make rs9395066(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 45127426 |
| Gene | SUPT3H |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9395066 |
| dbSNP (classic) | rs9395066 |
| ClinGen | rs9395066 |
| ebi | rs9395066 |
| HLI | rs9395066 |
| Exac | rs9395066 |
| Gnomad | rs9395066 |
| Varsome | rs9395066 |
| LitVar | rs9395066 |
| Map | rs9395066 |
| PheGenI | rs9395066 |
| Biobank | rs9395066 |
| 1000 genomes | rs9395066 |
| hgdp | rs9395066 |
| ensembl | rs9395066 |
| geneview | rs9395066 |
| scholar | rs9395066 |
| rs9395066 | |
| pharmgkb | rs9395066 |
| gwascentral | rs9395066 |
| openSNP | rs9395066 |
| 23andMe | rs9395066 |
| SNPshot | rs9395066 |
| SNPdbe | rs9395066 |
| MSV3d | rs9395066 |
| GWAS Ctlg | rs9395066 |
| GMAF | 0.4568 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18391951] |
| Trait | Height |
| Title | Many sequence variants affecting diversity of adult human height |
| Risk Allele | C |
| P-val | 0.0000079999999999999996 |
| Odds Ratio | 3.50 [1.93-5.07] % SD taller |
